510(k) Report

510(k) · Cleared

Recalled · Class II · 2014

Zoll X Series

K112432510(k) TraditionalCleared Mar 21, 2012211-day reviewClass III21 CFR 870.5310Recalls 2

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly, last Nov 3, 2026

Zoll Medical Corporation, World Wide Headquarters · MKJ Automated External Defibrillators (Non-Wearable)

Cleared on Mar 21, 2012 as substantially equivalent to K102468 (Zoll Medical Corporation, World Wide Headquarters, 2010) and 6 other predicates after a 211-day review. Its family tree reaches back 13 generations to 1997. 2 of the 90 devices in its family, counting itself, have a Class I recall. 8 later devices descend from it. It has been recalled 2 times.

Decided
Mar 21, 2012
Review
211 days
Class
Class III
Product code
MKJ
Recalls
2
Predicates
7

Its longest line of descent runs back 13 generations to K962603 (1997). 81 ancestors in all, the oldest K853990 (1985). 8 later devices descend from it, 3 citing it directly. 2 of the 90 devices in this family, counting this one, have a Class I recall.

Other ancestors, by year clearedDescendants, by year cleared 2011: 1 other ancestor2010: 3 other ancestors2008: 2 other ancestors2007: 1 other ancestor2003: 6 other ancestors2006: 4 other ancestors2005: 5 other ancestors2004: 5 other ancestors2002: 6 other ancestors, 1 with a Class I recall12001: 2 other ancestors2000: 5 other ancestors1999: 6 other ancestors1992: 2 other ancestors1985: 1 other ancestor1996: 3 other ancestors1995: 5 other ancestors1990: 2 other ancestors1998: 4 other ancestors1997: 2 other ancestors, 1 with a Class I recall11991: 2 other ancestors1993: 1 other ancestor2012: 1 descendant cleared2014: 4 descendants cleared2018: 1 descendant cleared2021: 1 descendant cleared2024: 1 descendant clearedK962603 · Masimo Set MS-1 Pulse Oximeter & the Lnop Series of Sensors & Cables · Masimo Corp. · 1997K973887 · Masimo Set MS-1P Pulse Oximeter and the Lnop Series of Sensors and Cables · Masimo Corp. · 1998K982255 · Model 2000 Pulse Oximeter · Ivy Biomedical Systems, Inc. · 1998K991823 · N-395 Pulse Oximeter, Model N-395 · Nellcor Puritan Bennett, Inc. · 1999×2: 2 generations cleared close together, K012891 (2002), K021090 (2002) K033048 · Cas 740 Series Monitor, Models 740-1, 740M-1, 740-2MS, 740M-2MS, 740-2NL, 740M-2NL, 740-2NN, 740M-2NN, 740-3MS, 740M-3MS · Cas Medical Systems, Inc. · 2004 · recalledK050844 · 750C Series Monitor, Models 750C-2MS, 750CM-2MS, 750C-NNL, 750CM-2NL, 750C-3MS, 750CM-3MS, 750C-3NL, 750CM-3NL · Cas Medical Systems, Inc. · 2005K060065 · CAPNOSTREAM20 Two Parameter Bedside Monitor & CAPNOSTREAM10 One Parameter Bedside Monitor · Oridion Capnography, Inc. · 2006 · recalledK072295 · Capnostream 20 with A2 Adaptive Averaging Software · Oridion Capnography, Inc. · 2007K082268 · CAPNOSTREAM20 with Integrated Pulmonary Index · Oridion Capnography, Inc. · 2009 · recalledK091241 · Masimo Rainbow Set Radical 7 Pulse CO-Oximeter; Rad 87 Pulse CO-Oximeter · Masimo Corporation · 2009K100428 · Masimo Rainbow Set Radical 7R Pulse CO-Oximeter · Masimo Corporation · 20101990200020102020
Other ancestors, by generationDescendants, by generation 1 generation back: 6 other ancestors2 generations back: 6 other ancestors3 generations back: 16 other ancestors4 generations back: 12 other ancestors, 1 with a Class I recall15 generations back: 15 other ancestors6 generations back: 6 other ancestors, 1 with a Class I recall17 generations back: 5 other ancestors8 generations back: 2 other ancestors 1 generation forward: 3 descendants2 generations forward: 3 descendants3 generations forward: 1 descendant4 generations forward: 1 descendant K100428 · Masimo Rainbow Set Radical 7R Pulse CO-Oximeter · Masimo Corporation · 2010K091241 · Masimo Rainbow Set Radical 7 Pulse CO-Oximeter; Rad 87 Pulse CO-Oximeter · Masimo Corporation · 2009K082268 · CAPNOSTREAM20 with Integrated Pulmonary Index · Oridion Capnography, Inc. · 2009 · recalledK072295 · Capnostream 20 with A2 Adaptive Averaging Software · Oridion Capnography, Inc. · 2007K060065 · CAPNOSTREAM20 Two Parameter Bedside Monitor & CAPNOSTREAM10 One Parameter Bedside Monitor · Oridion Capnography, Inc. · 2006 · recalledK050844 · 750C Series Monitor, Models 750C-2MS, 750CM-2MS, 750C-NNL, 750CM-2NL, 750C-3MS, 750CM-3MS, 750C-3NL, 750CM-3NL · Cas Medical Systems, Inc. · 2005K033048 · Cas 740 Series Monitor, Models 740-1, 740M-1, 740-2MS, 740M-2MS, 740-2NL, 740M-2NL, 740-2NN, 740M-2NN, 740-3MS, 740M-3MS · Cas Medical Systems, Inc. · 2004 · recalledK021090 · Oximax N-550 Pulse Oximeter,Model N-550 Pulse Oximeter · Nellcor Puritan Bennett, Inc. · 2002K012891 · Oximax Pulse Oximetry System with N-595 Pulse Oximeter and Oximax Sensors and Cables (Aka Accessories) · Nellcor Puritan Bennett, Inc. · 2002 · recalledK991823 · N-395 Pulse Oximeter, Model N-395 · Nellcor Puritan Bennett, Inc. · 1999K982255 · Model 2000 Pulse Oximeter · Ivy Biomedical Systems, Inc. · 1998K973887 · Masimo Set MS-1P Pulse Oximeter and the Lnop Series of Sensors and Cables · Masimo Corp. · 1998K962603 · Masimo Set MS-1 Pulse Oximeter & the Lnop Series of Sensors & Cables · Masimo Corp. · 1997−10−50
  1. Root · 13 generations backK962603 Masimo Set MS-1 Pulse Oximeter & the Lnop Series of Sensors & CablesMasimo Corp. · 1997
  2. 9 generations between
  3. 3 generations backK082268 CAPNOSTREAM20 with Integrated Pulmonary IndexOridion Capnography, Inc. · 2009 · Recalled
  4. 2 generations backK091241 Masimo Rainbow Set Radical 7 Pulse CO-Oximeter; Rad 87 Pulse…Masimo Corporation · 2009
  5. 1 generation backK100428 Masimo Rainbow Set Radical 7R Pulse CO-OximeterMasimo Corporation · 2010
  6. This deviceK112432 Zoll X SeriesZoll Medical Corporation, World Wide Headquarters · 2012
  7. Descendant · cites it directly · 4 of its ownK133269 Zoll X SeriesZoll Medical Corporation, World Wide Headquarters · 2014
  8. Descendant · cites it directly · 3 of its ownK121367 Zoll Propaq XMZOLL Medical Corporation · 2012 · Recalled
  9. Descendant · 2 generations on · 2 of its ownK180482 ZOLL Propaq MZOLL Medical Corporation · 2018
  10. Descendant · 2 generations on · 2 of its ownK141774 Zoll X SeriesZOLL Medical Corporation · 2014
  11. Descendant · 3 generations on · 1 of its ownK202375 ZOLL Propaq MZOLL Medical Corporation · 2021
Show all 13 generations
  1. Root · 13 generations backK962603 Masimo Set MS-1 Pulse Oximeter & the Lnop Series of Sensors & CablesMasimo Corp. · 1997
  2. 12 generations backK973887 Masimo Set MS-1P Pulse Oximeter and the Lnop Series of Sensors and…Masimo Corp. · 1998
  3. 11 generations backK982255 Model 2000 Pulse OximeterIvy Biomedical Systems, Inc. · 1998
  4. 10 generations backK991823 N-395 Pulse Oximeter, Model N-395Nellcor Puritan Bennett, Inc. · 1999
  5. 9 generations backK012891 Oximax Pulse Oximetry System with N-595 Pulse Oximeter and Oximax…Nellcor Puritan Bennett, Inc. · 2002 · Recalled
  6. 8 generations backK021090 Oximax N-550 Pulse Oximeter,Model N-550 Pulse OximeterNellcor Puritan Bennett, Inc. · 2002
  7. 7 generations backK033048 Cas 740 Series Monitor, Models 740-1, 740M-1, 740-2MS, 740M-2MS…Cas Medical Systems, Inc. · 2004 · Recalled
  8. 6 generations backK050844 750C Series Monitor, Models 750C-2MS, 750CM-2MS, 750C-NNL…Cas Medical Systems, Inc. · 2005
  9. 5 generations backK060065 CAPNOSTREAM20 Two Parameter Bedside Monitor & CAPNOSTREAM10 One…Oridion Capnography, Inc. · 2006 · Recalled
  10. 4 generations backK072295 Capnostream 20 with A2 Adaptive Averaging SoftwareOridion Capnography, Inc. · 2007
  11. 3 generations backK082268 CAPNOSTREAM20 with Integrated Pulmonary IndexOridion Capnography, Inc. · 2009 · Recalled
  12. 2 generations backK091241 Masimo Rainbow Set Radical 7 Pulse CO-Oximeter; Rad 87 Pulse…Masimo Corporation · 2009
  13. 1 generation backK100428 Masimo Rainbow Set Radical 7R Pulse CO-OximeterMasimo Corporation · 2010
  14. This deviceK112432 Zoll X SeriesZoll Medical Corporation, World Wide Headquarters · 2012

Showing 5 of 8 descendants. See all descendants

Descendants cleared per year

2012: 12014: 42018: 12021: 12024: 1
2012high 4 (2014) · low 0 (2013)2026

Class I recalls in this family

Most influential descendants

Showing 5 of 8 · See all
  • K133269Zoll X SeriesZoll Medical Corporation, World Wide Headquarters · 2014 · cites it directly4descendants
  • K121367Zoll Propaq XMZOLL Medical Corporation · 2012 · cites it directly3descendants
  • K180482ZOLL Propaq MZOLL Medical Corporation · 2018 · 2 generations on2descendants
  • K141774Zoll X SeriesZOLL Medical Corporation · 2014 · 2 generations on2descendants
  • K202375ZOLL Propaq MZOLL Medical Corporation · 2021 · 3 generations on1descendant
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−13K962603Masimo Set MS-1 Pulse Oximeter & the Lnop Series of Sensors & CablesMasimo Corp.1997—
−12K973887Masimo Set MS-1P Pulse Oximeter and the Lnop Series of Sensors and CablesMasimo Corp.1998—
−11K982255Model 2000 Pulse OximeterIvy Biomedical Systems, Inc.1998—
−10K991823N-395 Pulse Oximeter, Model N-395Nellcor Puritan Bennett, Inc.1999—
−9K012891Oximax Pulse Oximetry System with N-595 Pulse Oximeter and Oximax Sensors and…Nellcor Puritan Bennett, Inc.20021
−8K021090Oximax N-550 Pulse Oximeter,Model N-550 Pulse OximeterNellcor Puritan Bennett, Inc.2002—
−7K033048Cas 740 Series Monitor, Models 740-1, 740M-1, 740-2MS, 740M-2MS, 740-2NL…Cas Medical Systems, Inc.20041
−6K050844750C Series Monitor, Models 750C-2MS, 750CM-2MS, 750C-NNL, 750CM-2NL…Cas Medical Systems, Inc.2005—
−5K060065CAPNOSTREAM20 Two Parameter Bedside Monitor & CAPNOSTREAM10 One Parameter…Oridion Capnography, Inc.20063
−4K072295Capnostream 20 with A2 Adaptive Averaging SoftwareOridion Capnography, Inc.2007—
−3K082268CAPNOSTREAM20 with Integrated Pulmonary IndexOridion Capnography, Inc.20099
−2K091241Masimo Rainbow Set Radical 7 Pulse CO-Oximeter; Rad 87 Pulse CO-OximeterMasimo Corporation2009—
−1K100428Masimo Rainbow Set Radical 7R Pulse CO-OximeterMasimo Corporation2010—
0 (this device)K112432Zoll X SeriesZoll Medical Corporation, World Wide Headquarters2012—
+1K133269Zoll X SeriesZoll Medical Corporation, World Wide Headquarters2014—
+1K121367Zoll Propaq XMZOLL Medical Corporation20121
+2K180482ZOLL Propaq MZOLL Medical Corporation2018—
+2K141774Zoll X SeriesZOLL Medical Corporation2014—
+3K202375ZOLL Propaq MZOLL Medical Corporation2021—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
198510
199020
199120
199220
199310
199550
199630
199721
199840
199960
200050
200120
200261
200360
200450
200550
200640
200710
200820
201030
201110

Descendants by year cleared

Year clearedDevicesWith a Class I recall
201210
201440
201810
202110
202410
FIG. 1 — Lineage of K112432, 1997–2024Source: FDA 510(k) summaries, read by 510(k) Report · How lineage is built

Get the monthly Device Review Tracker

Notable FDA decisions, review times and new Class I recalls. See an issue.

Sources: FDA 510(k) database (decision fields), the FDA summary (predicates and indications), FDA recall and enforcement reports, and MAUDE; processed by 510(k) Report. Verify on FDA.gov · Methodology and accuracy.

2 devices in this family have a Class I recall. A 510(k) Report weighs predicate choices, recall history and review times for a new device like this one.

  • Candidate predicates for a device like this, rankedin the report
  • Recall history across each candidate’s familyin the report
Get a 510(k) Report

What was it cleared against? (7)

Devices the submitter claimed this one is substantially equivalent to (*), and reference devices cited for a specific test or feature (†), as written in the FDA summary.

TypeNumberDeviceApplicantDecidedRecalls
*K102468Zoll Propaq MD
Summary page 6
…/I2q3z-2, f6 The ZOLL X Series is substantially equivalent to the features and functions of the predicate units: ZOLL Propaq MD (K 102468), ZOLL E Series (K072923, KI110168, K070455), Inovise Audicor 12-lead Interpretive algorithm (K032 145), Masimo Rainbow MX3 modul…
Zoll Medical Corporation, World Wide Headquarters2010—
*K072923Zoll E Series Defibrillator
Summary page 6
…/I2q3z-2, f6 The ZOLL X Series is substantially equivalent to the features and functions of the predicate units: ZOLL Propaq MD (K 102468), ZOLL E Series (K072923, KI110168, K070455), Inovise Audicor 12-lead Interpretive algorithm (K032 145), Masimo Rainbow MX3 module (K100428) and Oridion m…
Zoll Medical Corporation, World Wide Headquarters2008—
*K110168Zoll E Series with 2010 Aha Guidlines Software Update
Summary page 6
…/I2q3z-2, f6 The ZOLL X Series is substantially equivalent to the features and functions of the predicate units: ZOLL Propaq MD (K 102468), ZOLL E Series (K072923, KI110168, K070455), Inovise Audicor 12-lead Interpretive algorithm (K032 145), Masimo Rainbow MX3 module (K100428) and Oridion microMediCO…
Zoll Medical Corporation, World Wide Headquarters2011—
*K070455Zoll E Series with See-Thru CPR
Summary page 6
…2, f6 The ZOLL X Series is substantially equivalent to the features and functions of the predicate units: ZOLL Propaq MD (K 102468), ZOLL E Series (K072923, KI110168, K070455), Inovise Audicor 12-lead Interpretive algorithm (K032 145), Masimo Rainbow MX3 module (K100428) and Oridion microMediCO2 module…
Zoll Medical Corporation, World Wide Headquarters2007—
*K032145Audicor Upgrade System
Summary page 6
…the features and functions of the predicate units: ZOLL Propaq MD (K 102468), ZOLL E Series (K072923, KI110168, K070455), Inovise Audicor 12-lead Interpretive algorithm (K032 145), Masimo Rainbow MX3 module (K100428) and Oridion microMediCO2 module (K094012) reviewed and cleared by the FDA. Comparison of T…
Inovise Medical, Inc.2003—
*K100428Masimo Rainbow Set Radical 7R Pulse CO-Oximeter
Summary page 6
…icate units: ZOLL Propaq MD (K 102468), ZOLL E Series (K072923, KI110168, K070455), Inovise Audicor 12-lead Interpretive algorithm (K032 145), Masimo Rainbow MX3 module (K100428) and Oridion microMediCO2 module (K094012) reviewed and cleared by the FDA. Comparison of Technological Characteristics The ZOLL…
Masimo Corporation2010—
*K094012CAPNOSTREAM20 with MICROMEDICO2 Module
Summary page 6
…LL E Series (K072923, KI110168, K070455), Inovise Audicor 12-lead Interpretive algorithm (K032 145), Masimo Rainbow MX3 module (K100428) and Oridion microMediCO2 module (K094012) reviewed and cleared by the FDA. Comparison of Technological Characteristics The ZOLL X Series utilizes the same features and f…
Oridion Capnography, Inc.2010—

What descends from it? (8)

3 later devices cite it directly; ranked here by how many devices descend from each in turn.

NumberDeviceApplicantDecidedDescendants
K133269Zoll X SeriesZoll Medical Corporation, World Wide Headquarters20144
K121367Zoll Propaq XMZOLL Medical Corporation20123
K133484Zoll X SeriesZoll Medical Corp20141

Has anything in its family been recalled? (2 Class I)

Recalls of this device

DateClassRecallRoot causeReason
Mar 5, 2014Class IIZ-1311-2014Software designDefibrillator/Pacemaker/Monitor May Latch in a Continuous Device Reset Loop and cannot be used
Aug 16, 2012Class IIZ-2401-2012Process controlShipped with incorrect software

Relatives with a Class I recall

Class I is FDA’s most serious recall class. A recall in the family tree is context for this device, not evidence about it.

  • K022732Infant/Child Reduced Energy ElectrodesMedtronic Physio-Control Corp. · 2002 · 4 generations back · ◆ in the 2002 ancestors bar of FIG. 12 Class I recalls
  • K970209Capnocheck PlusBci Intl., Inc. · 1997 · 6 generations back · ◆ in the 1997 ancestors bar of FIG. 11 Class I recall

What does this lineage say?

  • The line of descent spans 15 years and passes through 7 companies; a new generation was cleared every 11 months on median.
  • 18 of the 81 ancestors have a recall of any class; 2 have a Class I recall.
  • Of its descendants, K133269 (Zoll Medical Corporation, World Wide Headquarters, 2014) has gone furthest, with 4 descendants of its own.

How does its category compare?

All MKJ devices

MKJ Automated External Defibrillators (Non-Wearable): FDA decisions, review times, recalls and adverse event reports over 20 years. 2012, this device’s year, is highlighted.

FDA decisions per year · MKJ

48in 2025

2007: 72008: 132009: 82010: 42011: 112012: 102013: 72014: 112015: 62017: 42018: 202019: 252020: 522021: 412022: 192023: 242024: 272025: 482026 (partial year): 31
2007high 52 (2020) · low 0 (2016)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · MKJ

156in 2015

2007: 69 days median2008: 141 days median2009: 165 days median2010: 250 days median2011: 36 days median2012: 197 days median2013: 191 days median2014: 196 days median2015: 156 days median
2007high 250 (2010) · low 36 (2011)2026

Receipt to decision; years with fewer than 3 clearances left blank.

Recalls per year · MKJ

1in 2025

2007: 122008: 242009: 372010: 352011: 72012: 5, 1 Class I2013: 42014: 24, 15 Class I2015: 12016: 2, 1 Class I2017: 6, 4 Class I2018: 32019: 6, 2 Class I2020: 22021: 42022: 32023: 112024: 52025: 12026 (partial year): 3
2007high 37 (2009) · low 1 (2015)2026

Class I (23 since 2007) Class II/III not classified

Adverse event reports per year · MKJ

13,315in 2025

2007: 3,9582008: 4,7522009: 6,7822010: 7,3992011: 8,1702012: 9,7322013: 14,9552014: 15,3992015: 16,1292016: 17,0622017: 16,6842018: 16,5912019: 16,8612020: 16,1972021: 16,3002022: 14,8672023: 13,7662024: 15,1092025: 13,315
2007high 17,062 (2016) · low 3,958 (2007)2025

MAUDE reports naming product code MKJ, not matched to any one device; reports are not rates.

View these four charts as a table
YearDecisionsMedian 510(k) review, daysRecalls (Class I)MAUDE reports
2007769123,958
200813141244,752
20098165376,782
20104250357,399
2011113678,170
2012101975 (1)9,732
20137191414,955
20141119624 (15)15,399
20156156116,129
20160—2 (1)17,062
20174—6 (4)16,684
201820—316,591
201925—6 (2)16,861
202052—216,197
202141—416,300
202219—314,867
202324—1113,766
202427—515,109
202548—113,315
202631—3—

What is it indicated for?

The X Series is intended for use by trained medical personnel who are familiar with basic monitoring, vital sign assessment, emergency cardiac care, and the use of the X Series. The X Series is also intended for use by (or on the order of) physicians at the scene of an emergency or in a hospital emergency room, intensive care unit, cardiac care unit, or other similar areas of a hospital. The usage may be in an ambulance or at the scene of an emergency.…

Read the full statement (1,128 words)

The X Series is intended for use by trained medical personnel who are familiar with basic monitoring, vital sign assessment, emergency cardiac care, and the use of the X Series. The X Series is also intended for use by (or on the order of) physicians at the scene of an emergency or in a hospital emergency room, intensive care unit, cardiac care unit, or other similar areas of a hospital. The usage may be in an ambulance or at the scene of an emergency. It is also intended to be used during the transport of patients. The X Series will be used primarily on patients experiencing symptoms of cardiac arrest or in post trauma situation. It may also be used whenever it is required to monitor any of those functions that are included (as options) in the device. The X Series unit can be used on pediatric patients (as described in the following table) and on adult patients (21 years of age or older) with and without heart dysfunction.

Pediatric Patient Subpopulation Approximate Age Range

Newborn (neonate) Birth to 1 month of age.

Infant 1 month to 2 years of age.

Child 2 to 12 years of age.

Adolescent 12 to 21 years of age.

When the pediatric patient is less than 8 years of age or weighs less than 55 lbs. (25 kg.), use ZOLL pedi-padz® pediatric defibrillation electrodes. Do not delay therapy to determine the patient's exact age or weight.

Manual Defibrillation

Use of the X Series in the manual mode for external and internal defibrillation is indicated on victims of cardiac arrest where there is apparent lack of circulation as indicated by:

* Unconsciousness.

* Absence of breathing.

* Absence of pulse.

This product should be used only by qualified medical personnel for converting ventricular fibrillation and rapid ventricular tachycardia to sinus rhythm or other cardiac rhythms capable of producing hemodynamically significant heart beats.

The unit can also be used for synchronized cardioversion of certain atrial or ventricular arrhythmias. Qualified medical personnel must decide when synchronized cardioversion is appropriate.

The patient population will range from newborn (neonate) to adult.

Semiautomatic Operation (AED)

X Series products are designed for use by emergency care personnel who have completed training and certification requirements applicable to the use of a defibrillator where the device operator controls delivery of shocks to the patient.

They are specifically designed for use in early defibrillation programs where the delivery of a defibrillator shock during resuscitation involving CPR, transportation, and definitive care are incorporated into a medically-approved patient care protocol.

Use of the X Series in the Semiautomatic mode for defibrillation is indicated on victims of cardiac arrest where there is apparent lack of circulation as indicated by:

* Unconsciousness.

* Absence of breathing.

* Absence of pulse.

Specifications for the ECG rhythm analysis function are provided in the Operator's Manual section "EGG Analysis Algorithm Accuracy" on page A-33.

When the patient is less than 8 years of age or weighs less that 55 lbs. (25 Kg), you must use ZOLL pediatric defibrillation electrodes. Do not delay therapy to determine patient's exact age or weight.

ECG Monitoring

The X Series is intended for use to monitor and/or record 3-, 5-, or 12-lead EGG waveform and heart rate, and to alarm when heart rate is above or below limits set by the operator. The patient population will range from newborn (neonate) to adult, with and without heart dysfunction.

CPR Monitoring

The CPR monitoring function provides visual and audio feedback designed to encourage rescuers to perform chest compressions at the AHA/ERC recommended rate of 100 compressions per minute. Voice and visual prompts encourage a minimum compression depth of at least 1.5 (3.8 cm) or 2.0 inches (5.0 cm), depending on the configuration, for adult patients. The CPR monitoring function is not intended for use on patients under 8 years of age.

External Transcutaneous Pacing

This product can be used for temporary external cardiac pacing in conscious or unconscious patients as an alternative to endocardial stimulation. The purposes of pacing include:

* Resuscitation from standstill or bradycardia of any etiology:

* As a standby when standstill or bradycardia might be expected:

* Suppression of tachycardia.

* Pediatric pacing.

Non-invasive Blood Pressure Monitoring

The X Series is intended for use to make non-invasive measurements of arterial pressure and heart rate, and to alarm if either parameter is outside of the limits set by the user. Measurements are made using an inflatable cuff on the patient's arm or leg. The patient population will range from newborn (neonate) to adult.

Temperature Monitoring

The X Series is intended for use to make continuous temperature measurements of rectal, esophageal, or surface temperatures, and to alarm if the temperature is outside of the limits set by the user. The patient population will range from newborn (neonate) to adult.

SpO2 Monitoring

The X Series pulse CO-oximeter, with Masimo Rainbow SET technology and the Rainbow series of sensors, is intended for use for continuous noninvasive monitoring of functional oxygen saturation of arterial hemoglobin (SpO2), pulse rate, carboxyhemoglobin saturation (SpCO), and/or methemoglobin saturation (SpMet). The pulse CO-oximeter and accessories are indicated for use on adult, pediatric, and neonatal patients during both no motion and motion conditions, and for patients who are well or poorly perfused, in hospitals, hospital-type facilities, or in mobile environments.

Respiration Monitoring

The X Series is intended for use to continuously monitor respiration rate and to alarm if the rate falls outside of the range set by the operator. Because the measurement method actually measures respiratory effort, apnea episodes with continued respiratory effort (such as obstructive apnea) may not be detected. It is not intended to be used as an apnea monitor. The patient population will range from newborn (neonate) to adult.

CO2 Monitoring

The X Series is intended for use to make continuous noninvasive measurement and monitoring of carbon dioxide concentration of the expired and inspired breath and breath rate. The patient population will range from newborn (neonate) to adult.

Invasive Pressure Monitoring

The X Series is intended for use to display and make continuous invasive pressure measurements from any compatible pressure transducer. The primary intended uses are arterial blood pressure, central venous pressure and intracranial pressure monitoring. Any contraindications of the particular transducer selected by the user shall apply. The patient population will range from newborn (neonate) to adult.

12-Lead Analysis

The 12-lead ECG Analysis is intended for use in acquiring, analyzing and reporting EG data, and to provide interpretation of the data for consideration by caregivers. The interpretations of EGG data offered by the device are only significant when used in conjunction with caregiver overread as well as consideration of all other relevant patient data. The 12-lead EGG Analysis is intended for use on adults (> 18 years of age).

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K112432: Zoll X Series.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 5, 2026. https://510kreport.com/device/K112432

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Record history
  • FDA decision record loaded May 2, 2026
  • Summary read Oct 13, 2026 (extraction version 9eaa42aa01ed)
  • Lineage and recalls computed Nov 3, 2026
  • Page last updated Nov 3, 2026