510(k) Report

510(k) · Cleared

Cleared

Zoll Propaq MD

K102468510(k) SpecialCleared Sep 30, 201031-day reviewClass II21 CFR 870.5300

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 · LDD Dc-Defibrillator, Low-Energy, (Including Paddles)

Cleared on Sep 30, 2010 as substantially equivalent to K100654 (Zoll Medical Corporation, World Wide Headquarters, 2010) after a 31-day review. Its family tree reaches back 10 generations to 1997. 2 of the 66 devices in its family, counting itself, have a Class I recall. 9 later devices descend from it.

Decided
Sep 30, 2010
Review
31 days
Class
Class II
Product code
LDD
Recalls
None
Predicates
1

Its longest line of descent runs back 10 generations to K962603 (1997). 56 ancestors in all, the oldest K893221 (1990). 9 later devices descend from it, 1 citing it directly. 2 of the 66 devices in this family, counting this one, have a Class I recall.

Other ancestors, by year clearedDescendants, by year cleared 2006: 1 other ancestor2004: 3 other ancestors2002: 5 other ancestors, 1 with a Class I recall12001: 2 other ancestors2005: 3 other ancestors2003: 3 other ancestors2000: 3 other ancestors1999: 6 other ancestors1996: 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 ancestor1992: 1 other ancestor2012: 2 descendants 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 · recalledK100654 · Zoll Propaq MD · Zoll Medical Corporation, World Wide Headquarters · 20101990200020102020
Other ancestors, by generationDescendants, by generation 2 generations back: 4 other ancestors3 generations back: 10 other ancestors4 generations back: 18 other ancestors5 generations back: 6 other ancestors, 2 with a Class I recall26 generations back: 6 other ancestors7 generations back: 2 other ancestors 1 generation forward: 1 descendant2 generations forward: 3 descendants3 generations forward: 3 descendants4 generations forward: 1 descendant5 generations forward: 1 descendant K100654 · Zoll Propaq MD · Zoll Medical Corporation, World Wide Headquarters · 2010K060065 · 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+5
  1. Root · 10 generations backK962603 Masimo Set MS-1 Pulse Oximeter & the Lnop Series of Sensors & CablesMasimo Corp. · 1997
  2. 6 generations between
  3. 3 generations backK050844 750C Series Monitor, Models 750C-2MS, 750CM-2MS, 750C-NNL…Cas Medical Systems, Inc. · 2005
  4. 2 generations backK060065 CAPNOSTREAM20 Two Parameter Bedside Monitor & CAPNOSTREAM10 One…Oridion Capnography, Inc. · 2006 · Recalled
  5. 1 generation backK100654 Zoll Propaq MDZoll Medical Corporation, World Wide Headquarters · 2010
  6. This deviceK102468 Zoll Propaq MDZoll Medical Corporation, World Wide Headquarters · 2010
  7. Descendant · cites it directly · 8 of its ownK112432 Zoll X SeriesZoll Medical Corporation, World Wide Headquarters · 2012 · Recalled
  8. Descendant · 2 generations on · 4 of its ownK133269 Zoll X SeriesZoll Medical Corporation, World Wide Headquarters · 2014
  9. Descendant · 2 generations on · 3 of its ownK121367 Zoll Propaq XMZOLL Medical Corporation · 2012 · Recalled
  10. Descendant · 3 generations on · 2 of its ownK180482 ZOLL Propaq MZOLL Medical Corporation · 2018
  11. Descendant · 3 generations on · 2 of its ownK141774 Zoll X SeriesZOLL Medical Corporation · 2014
Show all 10 generations
  1. Root · 10 generations backK962603 Masimo Set MS-1 Pulse Oximeter & the Lnop Series of Sensors & CablesMasimo Corp. · 1997
  2. 9 generations backK973887 Masimo Set MS-1P Pulse Oximeter and the Lnop Series of Sensors and…Masimo Corp. · 1998
  3. 8 generations backK982255 Model 2000 Pulse OximeterIvy Biomedical Systems, Inc. · 1998
  4. 7 generations backK991823 N-395 Pulse Oximeter, Model N-395Nellcor Puritan Bennett, Inc. · 1999
  5. 6 generations backK012891 Oximax Pulse Oximetry System with N-595 Pulse Oximeter and Oximax…Nellcor Puritan Bennett, Inc. · 2002 · Recalled
  6. 5 generations backK021090 Oximax N-550 Pulse Oximeter,Model N-550 Pulse OximeterNellcor Puritan Bennett, Inc. · 2002
  7. 4 generations backK033048 Cas 740 Series Monitor, Models 740-1, 740M-1, 740-2MS, 740M-2MS…Cas Medical Systems, Inc. · 2004 · Recalled
  8. 3 generations backK050844 750C Series Monitor, Models 750C-2MS, 750CM-2MS, 750C-NNL…Cas Medical Systems, Inc. · 2005
  9. 2 generations backK060065 CAPNOSTREAM20 Two Parameter Bedside Monitor & CAPNOSTREAM10 One…Oridion Capnography, Inc. · 2006 · Recalled
  10. 1 generation backK100654 Zoll Propaq MDZoll Medical Corporation, World Wide Headquarters · 2010
  11. This deviceK102468 Zoll Propaq MDZoll Medical Corporation, World Wide Headquarters · 2010

Showing 5 of 9 descendants. See all descendants

Descendants cleared per year

2012: 22014: 42018: 12021: 12024: 1
2012high 4 (2014) · low 0 (2013)2026

Class I recalls in this family

Most influential descendants

Showing 5 of 9 · See all
  • K112432Zoll X SeriesZoll Medical Corporation, World Wide Headquarters · 2012 · cites it directly8descendants
  • K133269Zoll X SeriesZoll Medical Corporation, World Wide Headquarters · 2014 · 2 generations on4descendants
  • K121367Zoll Propaq XMZOLL Medical Corporation · 2012 · 2 generations on3descendants
  • K180482ZOLL Propaq MZOLL Medical Corporation · 2018 · 3 generations on2descendants
  • K141774Zoll X SeriesZOLL Medical Corporation · 2014 · 3 generations on2descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−10K962603Masimo Set MS-1 Pulse Oximeter & the Lnop Series of Sensors & CablesMasimo Corp.1997—
−9K973887Masimo Set MS-1P Pulse Oximeter and the Lnop Series of Sensors and CablesMasimo Corp.1998—
−8K982255Model 2000 Pulse OximeterIvy Biomedical Systems, Inc.1998—
−7K991823N-395 Pulse Oximeter, Model N-395Nellcor Puritan Bennett, Inc.1999—
−6K012891Oximax Pulse Oximetry System with N-595 Pulse Oximeter and Oximax Sensors and…Nellcor Puritan Bennett, Inc.20021
−5K021090Oximax N-550 Pulse Oximeter,Model N-550 Pulse OximeterNellcor Puritan Bennett, Inc.2002—
−4K033048Cas 740 Series Monitor, Models 740-1, 740M-1, 740-2MS, 740M-2MS, 740-2NL…Cas Medical Systems, Inc.20041
−3K050844750C Series Monitor, Models 750C-2MS, 750CM-2MS, 750C-NNL, 750CM-2NL…Cas Medical Systems, Inc.2005—
−2K060065CAPNOSTREAM20 Two Parameter Bedside Monitor & CAPNOSTREAM10 One Parameter…Oridion Capnography, Inc.20063
−1K100654Zoll Propaq MDZoll Medical Corporation, World Wide Headquarters2010—
0 (this device)K102468Zoll Propaq MDZoll Medical Corporation, World Wide Headquarters2010—
+1K112432Zoll X SeriesZoll Medical Corporation, World Wide Headquarters20122
+2K133269Zoll X SeriesZoll Medical Corporation, World Wide Headquarters2014—
+2K121367Zoll Propaq XMZOLL Medical Corporation20121
+3K180482ZOLL Propaq MZOLL Medical Corporation2018—
+3K141774Zoll X SeriesZOLL Medical Corporation2014—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
199020
199120
199210
199310
199550
199630
199721
199840
199960
200030
200120
200251
200330
200430
200530
200610

Descendants by year cleared

Year clearedDevicesWith a Class I recall
201220
201440
201810
202110
202410
FIG. 1 — Lineage of K102468, 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.

Top candidate predicates for a new LDD device

  1. #1 K200849 Tempus LS - Manualscore 1.3 · 13 generations · no Class I recall
  2. #2 Held for the reportin the report
Get a 510(k) Report

What was it cleared against? (1)

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
*K100654Zoll Propaq MD
Summary page 5
…4 of S Substantial Equivalence: Propaq MD with the SmartCuf feature issubstantially equivalent to the features and functions of the predicate Propaq MD (k100654) reviewed and cleared by the FDA. Comparison of Technological Characteristics Propaq MD with the SmartCuf feature utilizes the s…
Zoll Medical Corporation, World Wide Headquarters2010—

Also cleared against K100654: 1 other device →

What descends from it? (9)

1 later device cites it directly; ranked here by how many devices descend from each in turn.

NumberDeviceApplicantDecidedDescendants
K112432Zoll X SeriesZoll Medical Corporation, World Wide Headquarters20128

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

No FDA recall names this device.

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 · 5 generations back · ◆ in the 2002 ancestors bar of FIG. 12 Class I recalls
  • K970209Capnocheck PlusBci Intl., Inc. · 1997 · 5 generations back · ◆ in the 1997 ancestors bar of FIG. 11 Class I recall

What does this lineage say?

  • The line of descent spans 13 years and passes through 6 companies; a new generation was cleared every 11 months on median.
  • 13 of the 56 ancestors have a recall of any class; 2 have a Class I recall.
  • Of its descendants, K112432 (Zoll Medical Corporation, World Wide Headquarters, 2012) has gone furthest, with 8 descendants of its own.
  • 1 other device also cites its predicate K100654.

How does its category compare?

All LDD devices

LDD Dc-Defibrillator, Low-Energy, (Including Paddles): FDA decisions, review times, recalls and adverse event reports over 20 years. 2010, this device’s year, is highlighted.

FDA decisions per year · LDD

1in 2021

2008: 22010: 22011: 42014: 12015: 12019: 12020: 12021: 1
2007high 4 (2011) · low 0 (2007)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · LDD

124in 2011

2011: 124 days median
2007high 124 (2011)2026

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

Recalls per year · LDD

2in 2024

2008: 112009: 12011: 12014: 2, 2 Class I2020: 12022: 12024: 2
2007high 11 (2008) · low 0 (2007)2026

Class I (2 since 2007) Class II/III not classified

Adverse event reports per year · LDD

74in 2025

2007: 5502008: 1,2142009: 1,0572010: 6352011: 3862012: 3982013: 6022014: 4812015: 862016: 582017: 492018: 282019: 342020: 192021: 222022: 802023: 2642024: 1602025: 74
2007high 1,214 (2008) · low 19 (2020)2025

MAUDE reports naming product code LDD, 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
20070—0550
20082—111,214
20090—11,057
20102—0635
201141241386
20120—0398
20130—0602
20141—2 (2)481
20151—086
20160—058
20170—049
20180—028
20191—034
20201—119
20211—022
20220—180
20230—0264
20240—2160
20250—074
20260—0—

What is it indicated for?

The Propaq MD 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 Propaq MD. The Propaq MD 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…

Read the full statement (1,011 words)

The Propaq MD 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 Propaq MD. The Propaq MD 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 Propaq MD 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 Propaq MD 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 pedispodz® pediatric dlefibrillation electrodes. Do not delay therapy to determine the patient's exact age or weight.

Manual Defibrillation

Use of the Propaq MD in the manual mode for external and internal dlefibrillation 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.

ECG Monitoring

The Propaq MD is intended for use to monitor and/or record 3-, 5-, or 12-lead ECG 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.

External Transcutaneous Pacing

This product can be used for temporary external cardiac pacing in conscious or unconscious patients as an alternative to enclocardial stimulation.

The purposes of pacing include:

* Resuscitation from standstill or bradycardia of any etiology:

Noninvasive pacing has been used for resuscitation from cardiac standstill, reflex vagal standstill, drug-induced standstill (due to procainamide, quinidine, digitalis, b-blockers, verapamnil, etc.) and unexpected circulatory arrest (due to anesthesia, surgery, angiography, and other therapeutic or diagnostic procedures). It has also been used for temporary acceleration of bradycardia in Stokes-Adams disease and sick-sinus syndrome. It is safer, more reliable, and more rapidly applied in an emergency than endlocardial or other temporary electrodes.

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

Noninvasive pacing can be useful as a standby when cardiac arrest or symptomatic bradycardia might be expected due to acute myocardial infarction, drug toxicity, anesthesia, or surgery. It is also useful as a temporary treatment in patients awaiting pacemaker implants or the introduction of transvenous therapy. In standby pacing applications, noninvasive pacing might provide an alternative to transvenous therapy that avoids the risks of displacement, infection, hemorrhage, embolization, perforation, phlebitis, and mechanicai or electrical stimulation of ventricular tachycardia or fibrillation associated with endlocardial pacing.

* Suppression of tachycardia.

Increased heart rates in response to external pacing often suppress ventricular ectopic activity and might prevent tachycardia.

* Pediatric pacing.

Pacing can be performed on pediatric patients weighing 33 lbs. (15 kg.) or less using ZOLL pediatric hands-free therapy electrode pads. Prolonged pacing (in excess of 30 minutes), particularly in neonates, could cause burns. Periodic inspection of underlying skin is recommended.

Non-Invasive Blood Pressure Monitoring

The Propaq MD 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 Propaq MD 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 Propaq MD is intended for use to monitor pulse rate and oxygen saturation of arteriolar hemoglobin, and to alarm if either parameter is outside of the limits set by the user. Measurements are made non-invasively at remote sites such as a finger, toe, ear lobe, bridge of nose, etc. The patient population will range from newborn (neonate) to adult.

Respiration Monitoring

The Propaq MD 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.

C02 Monitoring

The Propaq MD 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 Propaq MD 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 contraindlications of the particular transducer selected by the user shall apply. The patient population will range from newborn (neonate) to adult.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K102468: Zoll Propaq MD.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 3, 2026. https://510kreport.com/device/K102468

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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