510(k) Report

510(k) · Cleared

Cleared

Equivital, Model EQ-01

K061993510(k) TraditionalCleared Nov 3, 2006112-day reviewClass II21 CFR 870.1025

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

Hidalgo Limited · MHX Monitor, Physiological, Patient (With Arrhythmia Detection Or Alarms)

Cleared on Nov 3, 2006 as substantially equivalent to K030795 (Gmp/Companies, Inc., 2003) and 5 other predicates after a 112-day review. Its family tree reaches back 5 generations to 1997. 99 later devices descend from it.

Decided
Nov 3, 2006
Review
112 days
Class
Class II
Product code
MHX
Recalls
None
Predicates
6

Its longest line of descent runs back 5 generations to K962603 (1997). 22 ancestors in all, the oldest K891104 (1989). 99 later devices descend from it, 3 citing it directly.

Other ancestors, by year clearedDescendants, by year cleared 2005: 2 other ancestors2004: 1 other ancestor2003: 1 other ancestor2000: 2 other ancestors1999: 2 other ancestors1998: 1 other ancestor1996: 2 other ancestors1995: 1 other ancestor1994: 1 other ancestor1992: 1 other ancestor1993: 1 other ancestor1991: 1 other ancestor1989: 1 other ancestor2012: 2 descendants cleared2010: 1 descendant cleared2008: 1 descendant cleared2011: 1 descendant cleared2016: 2 descendants cleared2015: 3 descendants cleared2014: 1 descendant cleared2017: 5 descendants cleared2013: 1 descendant cleared2020: 8 descendants cleared2019: 9 descendants cleared2018: 5 descendants cleared2022: 8 descendants cleared2025: 15 descendants cleared2023: 13 descendants cleared2021: 4 descendants cleared2024: 12 descendants cleared2026: 8 descendants 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. · 1999K012451 · Propaq Encore Models 202, 204, 206; Propaq CS Models 242, 244, 246 · Welch Allyn Protocol, Inc. · 20011990200020102020
Other ancestors, by generationDescendants, by generation 1 generation back: 5 other ancestors2 generations back: 8 other ancestors3 generations back: 4 other ancestors 1 generation forward: 3 descendants2 generations forward: 5 descendants3 generations forward: 9 descendants4 generations forward: 16 descendants5 generations forward: 22 descendants6 generations forward: 15 descendants7 generations forward: 19 descendants8 generations forward: 7 descendants9 generations forward: 3 descendants K012451 · Propaq Encore Models 202, 204, 206; Propaq CS Models 242, 244, 246 · Welch Allyn Protocol, Inc. · 2001K991823 · 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. · 1997−50+5
  1. Root · 5 generations backK962603 Masimo Set MS-1 Pulse Oximeter & the Lnop Series of Sensors & CablesMasimo Corp. · 1997
  2. 4 generations backK973887 Masimo Set MS-1P Pulse Oximeter and the Lnop Series of Sensors and…Masimo Corp. · 1998
  3. 3 generations backK982255 Model 2000 Pulse OximeterIvy Biomedical Systems, Inc. · 1998
  4. 2 generations backK991823 N-395 Pulse Oximeter, Model N-395Nellcor Puritan Bennett, Inc. · 1999
  5. 1 generation backK012451 Propaq Encore Models 202, 204, 206; Propaq CS Models 242, 244, 246Welch Allyn Protocol, Inc. · 2001
  6. This deviceK061993 Equivital, Model EQ-01Hidalgo Limited · 2006
  7. Descendant · cites it directly · 71 of its ownK113054 EquivitalHidalgo Limited · 2012
  8. Descendant · 2 generations on · 70 of its ownK141167 Vitalconnect Platform (Consisting of Vitalconnect Sensor, Relay…Vitalconnect, Inc. · 2014
  9. Descendant · 3 generations on · 43 of its ownK152139 Vital Connect Platform, HealthPatch MD, VitalPatchVitalconnect, Inc. · 2015
  10. Descendant · cites it directly · 22 of its ownK081140 VisensiaObs Medical · 2008
  11. Descendant · 3 generations on · 18 of its ownK190073 Wearable Device, Home Package in Carry Case with Homehub, Home…Current Health, Ltd. · 2019

Showing 5 of 99 descendants. See all descendants

Descendants cleared per year

2008: 12010: 12011: 12012: 22013: 12014: 12015: 32016: 22017: 52018: 52019: 92020: 82021: 42022: 82023: 132024: 122025: 152026: 8
2008high 15 (2025) · low 0 (2009)2026

Most influential descendants

Showing 5 of 99 · See all
  • K113054EquivitalHidalgo Limited · 2012 · cites it directly71descendants
  • K141167Vitalconnect Platform (Consisting of Vitalconnect Sensor, Relay Software Library and…Vitalconnect, Inc. · 2014 · 2 generations on70descendants
  • K152139Vital Connect Platform, HealthPatch MD, VitalPatchVitalconnect, Inc. · 2015 · 3 generations on43descendants
  • K081140VisensiaObs Medical · 2008 · cites it directly22descendants
  • K190073Wearable Device, Home Package in Carry Case with Homehub, Home Package in Carry Case…Current Health, Ltd. · 2019 · 3 generations on18descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−5K962603Masimo Set MS-1 Pulse Oximeter & the Lnop Series of Sensors & CablesMasimo Corp.1997—
−4K973887Masimo Set MS-1P Pulse Oximeter and the Lnop Series of Sensors and CablesMasimo Corp.1998—
−3K982255Model 2000 Pulse OximeterIvy Biomedical Systems, Inc.1998—
−2K991823N-395 Pulse Oximeter, Model N-395Nellcor Puritan Bennett, Inc.1999—
−1K012451Propaq Encore Models 202, 204, 206; Propaq CS Models 242, 244, 246Welch Allyn Protocol, Inc.2001—
0 (this device)K061993Equivital, Model EQ-01Hidalgo Limited2006—
+1K113054EquivitalHidalgo Limited2012—
+2K141167Vitalconnect Platform (Consisting of Vitalconnect Sensor, Relay Software…Vitalconnect, Inc.2014—
+3K152139Vital Connect Platform, HealthPatch MD, VitalPatchVitalconnect, Inc.2015—
+1K081140VisensiaObs Medical2008—
+3K190073Wearable Device, Home Package in Carry Case with Homehub, Home Package in…Current Health, Ltd.2019—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
198910
199110
199210
199310
199410
199510
199620
199810
199920
200020
200310
200410
200520

Descendants by year cleared

Year clearedDevicesWith a Class I recall
200810
201010
201110
201220
201310
201410
201530
201620
201750
201850
201990
202080
202140
202280
2023130
2024120
2025150
202680
FIG. 1 — Lineage of K061993, 1997–2026Source: FDA 510(k) summaries, read by 510(k) Report · How lineage is built

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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.

Planning a device in MHX? 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 MHX device

  1. #1 K251702 IntelliVue Patient Monitor MX750; IntelliVue…score 23.0 · 40 generations · no Class I recall
  2. #2 Held for the reportin the report
  3. #3 Held for the reportin the report
Get a 510(k) Report

What was it cleared against? (6)

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
*K030795Lifesyne Systems
Summary page 2
…hidalgo®eee Predicate Devices The device has been compared to the following predicates: GMP Wireless Medicine LifeSync TM - K030795 Dymedix Inc Re-usable Respiratory Effort Belt Sensor - K040605 Nexan Inc NX-300…
Gmp/Companies, Inc.20033
*K040605Dymedix Reusable Respiratory Effort Belt Sensor, Model 6015 and Dymedix Reusable Limb…
Summary page 2
…ates: GMP Wireless Medicine LifeSync TM - K030795 Dymedix Inc Re-usable Respiratory Effort Belt Sensor - K040605 Nexan Inc NX-300 - K003520 Protocol Systems Propaq Enc…
Dymedix, Inc.2004—
*K003520Nexan System, Model NX-300
Summary page 2
…30795 Dymedix Inc Re-usable Respiratory Effort Belt Sensor - K040605 Nexan Inc NX-300 - K003520 Protocol Systems Propaq Encore 200 - K012451 Respironics Actiheartl…
Nexan, Ltd.2000—
*K012451Propaq Encore Models 202, 204, 206; Propaq CS Models 242, 244, 246
Summary page 2
…40605 Nexan Inc NX-300 - K003520 Protocol Systems Propaq Encore 200 - K012451 Respironics Actiheartl - K052489 Vivometrics Life Shirt…
Welch Allyn Protocol, Inc.2001—
*K052489Actiheart
Summary page 2
…03520 Protocol Systems Propaq Encore 200 - K012451 Respironics Actiheartl - K052489 Vivometrics Life ShirtTM Real Time -K043604 Device Description The EquivitalTM Vita…
Respironics, Inc.2005—
*K043604Lifeshirt Real-Time with Vivomonitor Software
Summary page 2
…12451 Respironics Actiheartl - K052489 Vivometrics Life ShirtTM Real Time -K043604 Device Description The EquivitalTM Vital Signs Physiological Monitor comprises two components: i) A chest belt containing sk…
Vivometrics, Inc.2005—

Also cleared against K030795: 3 other devices →

What descends from it? (99)

See all 99

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

NumberDeviceApplicantDecidedDescendants
K113054EquivitalHidalgo Limited201271
K081140VisensiaObs Medical200822
K100040BioharnessZephyr Technology Corporation20103

Has anything in its family been recalled? (0 Class I)

No FDA recall names this device.

No ancestor or descendant has a Class I recall.

What does this lineage say?

  • The line of descent spans 9 years and passes through 5 companies; a new generation was cleared every 11 months on median.
  • 3 of the 22 ancestors have a recall of any class.
  • Of its descendants, K113054 (Hidalgo Limited, 2012) has gone furthest, with 71 descendants of its own.
  • 3 other devices also cite its predicate K030795.

How does its category compare?

All MHX devices

MHX Monitor, Physiological, Patient (With Arrhythmia Detection Or Alarms): FDA decisions, review times, recalls and adverse event reports over 20 years.

FDA decisions per year · MHX

8in 2025

2007: 152008: 162009: 132010: 202011: 122012: 162013: 212014: 132015: 142016: 132017: 142018: 112019: 72020: 112021: 52022: 152023: 82024: 52025: 82026 (partial year): 14
2007high 21 (2013) · low 5 (2021)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · MHX

192in 2025

2007: 96 days median2008: 58 days median2009: 57 days median2010: 90 days median2011: 81 days median2012: 88 days median2013: 120 days median2014: 248 days median2015: 203 days median2016: 149 days median2017: 134 days median2018: 203 days median2019: 243 days median2020: 196 days median2021: 195 days median2022: 189 days median2023: 229 days median2024: 181 days median2025: 192 days median2026 (partial year): 205 days median
2007high 248 (2014) · low 57 (2009)2026

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

Recalls per year · MHX

21so far in 2026, the most since 2007

2007: 32008: 22009: 72010: 132011: 162012: 112013: 142014: 62015: 52016: 72017: 62018: 122019: 62022: 62023: 32024: 32025: 152026 (partial year): 21
2007high 21 (2026) · low 0 (2020)2026

Class I (0 since 2007) Class II/III not classified

Adverse event reports per year · MHX

3,761in 2025

2007: 1312008: 2322009: 3822010: 9552011: 9492012: 6762013: 1,9972014: 1,6092015: 1,2842016: 1,1052017: 1,1152018: 2,1572019: 1,4622020: 1,7142021: 2,4232022: 1,4702023: 2,2542024: 2,8142025: 3,761
2007high 3,761 (2025) · low 131 (2007)2025

MAUDE reports naming product code MHX, 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
200715963131
200816582232
200913577382
2010209013955
2011128116949
2012168811676
201321120141,997
20141324861,609
20151420351,284
20161314971,105
20171413461,115
201811203122,157
2019724361,462
20201119601,714
2021519502,423
20221518961,470
2023822932,254
2024518132,814
20258192153,761
20261420521—

What is it indicated for?

The Equivital TM Vital Signs Physiological Monitor is an ambulatory multiparameter vital signs telemetry device intended for monitoring of adults (16 - 65years) in hospital care facilities, the home, workplace and alternate care settings.

The device consists of a chest belt harness and a body worn electronics module (SEM) supported by the chest belt.

The device collects and transmits ECG data and rate, respiration data and rate, skin temperature, body orientation and motion.

The monitor is indicated for use as a general patient monitor, to provide physiological information as part of an occupational welfare monitoring system, and for general research and performance measurement purposes.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K061993: Equivital, Model EQ-01.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 4, 2026. https://510kreport.com/device/K061993

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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