510(k) Report

510(k) · Cleared

Cleared

Hypervisor Central Monitoring System (Including Telemetry Monitoring System, TMS-6016)

K132036510(k) AbbreviatedCleared Jul 1, 2014365-day reviewClass II21 CFR 870.2300

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

Shenzhen Mindray Bio-Meidcal Electronics Co., Ltd. · MSX System, Network And Communication, Physiological Monitors

Cleared on Jul 1, 2014 as substantially equivalent to K080192 (Shenzhen Mindray Bio-Medical Electronics Co., Ltd., 2008) after a 365-day review. Its family tree reaches back 5 generations to 1994. 17 later devices descend from it.

Decided
Jul 1, 2014
Review
365 days
Class
Class II
Product code
MSX
Recalls
None
Predicates
1

Its longest line of descent runs back 5 generations to K933143 (1994). 21 ancestors in all, the oldest K781836 (1978). 17 later devices descend from it, 3 citing it directly.

Other ancestors, by year clearedDescendants, by year cleared 2007: 1 other ancestor2001: 1 other ancestor1996: 1 other ancestor1995: 3 other ancestors1994: 2 other ancestors1986: 1 other ancestor1978: 1 other ancestor1997: 1 other ancestor1990: 2 other ancestors1989: 2 other ancestors1991: 1 other ancestor2015: 2 descendants cleared2017: 2 descendants cleared2016: 1 descendant cleared2019: 1 descendant cleared2020: 1 descendant cleared2023: 2 descendants cleared2022: 1 descendant cleared2026: 3 descendants cleared2025: 2 descendants cleared2024: 2 descendants clearedK933143 · Model Eli 300 Electrocardiograph · Mortara Instrument, Inc. · 1994K962970 · Spacelabs Medical 12-Lead Diagnostic Ecg Analysis Option · Spacelabs Medical, Inc. · 1997K972502 · Spacelabs Medical Integrated Multiparameter Module 90496 · Spacelabs Medical, Inc. · 1998 · recalledK983996 · Spacelabs Medical Ultraview Digital Telemtry System · Spacelabs Medical, Inc. · 1999K080192 · Hypervisor VI Central Monitoring System (Including TMS) · Shenzhen Mindray Bio-Medical Electronics Co., Ltd. · 2008 · recalled19801990200020102020
Other ancestors, by generationDescendants, by generation 2 generations back: 1 other ancestor3 generations back: 6 other ancestors4 generations back: 5 other ancestors5 generations back: 4 other ancestors 1 generation forward: 3 descendants2 generations forward: 2 descendants3 generations forward: 1 descendant4 generations forward: 1 descendant5 generations forward: 4 descendants6 generations forward: 4 descendants7 generations forward: 2 descendants K080192 · Hypervisor VI Central Monitoring System (Including TMS) · Shenzhen Mindray Bio-Medical Electronics Co., Ltd. · 2008 · recalledK983996 · Spacelabs Medical Ultraview Digital Telemtry System · Spacelabs Medical, Inc. · 1999K972502 · Spacelabs Medical Integrated Multiparameter Module 90496 · Spacelabs Medical, Inc. · 1998 · recalledK962970 · Spacelabs Medical 12-Lead Diagnostic Ecg Analysis Option · Spacelabs Medical, Inc. · 1997K933143 · Model Eli 300 Electrocardiograph · Mortara Instrument, Inc. · 1994−50+5
  1. Root · 5 generations backK933143 Model Eli 300 ElectrocardiographMortara Instrument, Inc. · 1994
  2. 4 generations backK962970 Spacelabs Medical 12-Lead Diagnostic Ecg Analysis OptionSpacelabs Medical, Inc. · 1997
  3. 3 generations backK972502 Spacelabs Medical Integrated Multiparameter Module 90496Spacelabs Medical, Inc. · 1998 · Recalled
  4. 2 generations backK983996 Spacelabs Medical Ultraview Digital Telemtry SystemSpacelabs Medical, Inc. · 1999
  5. 1 generation backK080192 Hypervisor VI Central Monitoring System (Including TMS)Shenzhen Mindray Bio-Medical Electronics Co., Ltd. · 2008 · Recalled
  6. This deviceK132036 Hypervisor Central Monitoring System (Including Telemetry Monitoring…Shenzhen Mindray Bio-Meidcal Electronics Co., Ltd. · 2014
  7. Descendant · cites it directly · 14 of its ownK150632 Hypervisor IX Monitoring SystemShenzhen Mindray Bio-Medical Electronics Co., Ltd. · 2015 · Recalled
  8. Descendant · 2 generations on · 12 of its ownK162607 BeneVision Central Monitoring SystemShenzhen Mindray Bio-Medical Electronics Co., Ltd. · 2017 · Recalled
  9. Descendant · 3 generations on · 11 of its ownK183238 BeneVision Central Monitoring SystemShenzhen Mindray Bio-Medical Electronics Co., Ltd. · 2019
  10. Descendant · 4 generations on · 10 of its ownK193391 BeneVision Central Monitoring SystemShenzhen Mindray Bio-Medical Electronics Co., Ltd. · 2020 · Recalled
  11. Descendant · 5 generations on · 3 of its ownK220058 BeneVision Central Monitoring SystemShenzhen Mindray Bio-Medical Electronics Co., Ltd. · 2022 · Recalled

Showing 5 of 17 descendants. See all descendants

Descendants cleared per year

2015: 22016: 12017: 22019: 12020: 12022: 12023: 22024: 22025: 22026: 3
2015high 3 (2026) · low 0 (2018)2026

Most influential descendants

Showing 5 of 17 · See all
  • K150632Hypervisor IX Monitoring SystemShenzhen Mindray Bio-Medical Electronics Co., Ltd. · 2015 · cites it directly14descendants
  • K162607BeneVision Central Monitoring SystemShenzhen Mindray Bio-Medical Electronics Co., Ltd. · 2017 · 2 generations on12descendants
  • K183238BeneVision Central Monitoring SystemShenzhen Mindray Bio-Medical Electronics Co., Ltd. · 2019 · 3 generations on11descendants
  • K193391BeneVision Central Monitoring SystemShenzhen Mindray Bio-Medical Electronics Co., Ltd. · 2020 · 4 generations on10descendants
  • K220058BeneVision Central Monitoring SystemShenzhen Mindray Bio-Medical Electronics Co., Ltd. · 2022 · 5 generations on3descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−5K933143Model Eli 300 ElectrocardiographMortara Instrument, Inc.1994—
−4K962970Spacelabs Medical 12-Lead Diagnostic Ecg Analysis OptionSpacelabs Medical, Inc.1997—
−3K972502Spacelabs Medical Integrated Multiparameter Module 90496Spacelabs Medical, Inc.19983
−2K983996Spacelabs Medical Ultraview Digital Telemtry SystemSpacelabs Medical, Inc.1999—
−1K080192Hypervisor VI Central Monitoring System (Including TMS)Shenzhen Mindray Bio-Medical Electronics Co., Ltd.20082
0 (this device)K132036Hypervisor Central Monitoring System (Including Telemetry Monitoring System…Shenzhen Mindray Bio-Meidcal Electronics Co., Ltd.2014—
+1K150632Hypervisor IX Monitoring SystemShenzhen Mindray Bio-Medical Electronics Co., Ltd.20152
+2K162607BeneVision Central Monitoring SystemShenzhen Mindray Bio-Medical Electronics Co., Ltd.20171
+3K183238BeneVision Central Monitoring SystemShenzhen Mindray Bio-Medical Electronics Co., Ltd.2019—
+4K193391BeneVision Central Monitoring SystemShenzhen Mindray Bio-Medical Electronics Co., Ltd.20202
+5K220058BeneVision Central Monitoring SystemShenzhen Mindray Bio-Medical Electronics Co., Ltd.20221

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
197810
198610
198920
199020
199110
199420
199530
199610
199710
200110
200710

Descendants by year cleared

Year clearedDevicesWith a Class I recall
201520
201610
201720
201910
202010
202210
202320
202420
202520
202630
FIG. 1 — Lineage of K132036, 1994–2026Source: 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.

Planning a device in MSX? 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 MSX device

  1. #1 K242750 Central Stationscore 21.5 · 31 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? (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
*K080192Hypervisor VI Central Monitoring System (Including TMS)
Summary page 2
…Class 11 21 CFR Part 870.2910 Transmitters and Receivers, Physiological Signal, Radiofrequency ClassliI Legally Marketed Predicate Devices: K080192, HYPERVISOR VI Central Monitoring System (including Telemetry Monitoring System, TMS-60 16), Shenzhen Mindr…
Shenzhen Mindray Bio-Medical Electronics Co., Ltd.20082

Also cleared against K080192: 2 other devices →

What descends from it? (17)

See all 17

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

NumberDeviceApplicantDecidedDescendants
K150632Hypervisor IX Monitoring SystemShenzhen Mindray Bio-Medical Electronics Co., Ltd.201514
K161056Telemetry TransmitterEdan Instruments, Inc.20170
K150082Panorama Patient Monitoring NetworkShenzhen Mindray Bio-Medical Electronics Co., Ltd.20150

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 20 years and passes through 4 companies; a new generation was cleared every 2.9 years on median.
  • 4 of the 21 ancestors have a recall of any class.
  • Of its descendants, K150632 (Shenzhen Mindray Bio-Medical Electronics Co., Ltd., 2015) has gone furthest, with 14 descendants of its own.
  • 2 other devices also cite its predicate K080192.

How does its category compare?

All MSX devices

MSX System, Network And Communication, Physiological Monitors: FDA decisions, review times, recalls and adverse event reports over 20 years. 2014, this device’s year, is highlighted.

FDA decisions per year · MSX

4in 2025

2007: 42008: 12009: 12010: 32011: 72012: 42013: 22014: 32015: 52016: 32017: 22018: 42019: 42020: 52021: 32022: 52023: 32024: 42025: 42026 (partial year): 5
2007high 7 (2011) · low 1 (2008)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · MSX

295in 2025

2007: 58 days median2010: 43 days median2011: 72 days median2012: 145 days median2014: 165 days median2015: 138 days median2016: 174 days median2018: 111 days median2019: 92 days median2020: 193 days median2021: 227 days median2022: 177 days median2023: 244 days median2024: 212 days median2025: 295 days median2026 (partial year): 145 days median
2007high 295 (2025) · low 43 (2010)2026

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

Recalls per year · MSX

1in 2025

2007: 12008: 12009: 22010: 12011: 12012: 22015: 22017: 22018: 12022: 12025: 12026 (partial year): 2
2007high 2 (2009) · low 0 (2013)2026

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

Adverse event reports per year · MSX

19in 2025

2007: 52008: 62009: 72010: 142011: 32012: 42013: 172014: 322015: 312016: 112017: 162018: 152019: 152020: 252021: 172022: 182023: 102024: 322025: 19
2007high 32 (2014) · low 3 (2011)2025

MAUDE reports naming product code MSX, 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
200745815
20081—16
20091—27
2010343114
201177213
2012414524
20132—017
20143165032
20155138231
20163174011
20172—216
20184111115
2019492015
20205193025
20213227017
20225177118
20233244010
20244212032
20254295119
202651452—

What is it indicated for?

The CMS network transfers information between Hypervisor Central Monitoring System and other networked devices, It also allows information transfer between several CMS. Network connections consist aof hardwired network cables and/or WLAN connections. CMS can be used for remote monitor management, storing, printing, reviewing or processing of information from networked devices, and it is operated by medical personnel in hospitals or medical institutions.

Telemetry Monitoring System is a sub-system of CMS, intended to obtain ECG and SpO 2 physiological information from adult and pediatric patients, and send it to CMS via WMTS frequency within adefined coverage area.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K132036: Hypervisor Central Monitoring System (Including Telemetry Monitoring System, TMS-6016).” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K132036

Report an extraction error

Tell us what is wrong; we check it against the FDA summary.

Are you the manufacturer?

Send a correction or an update to this page, for example a newer model or a public statement about a recall.

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