# K062194: Hypervisor VI Central Monitoring System

- Pathway: 510(k) (Traditional)
- Applicant: Shenzhen Mindray Bio-Medical Electronics Co., Ltd.
- Decided: Apr 11, 2007 after 254 days
- Product code: MHX (Monitor, Physiological, Patient(With Arrhythmia Detection Or Alarms))
- Device class: 2
- Regulation: 21 CFR 870.1025
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 1 generation back to K011093 (2001). 1 ancestor in all.
25 later devices descend from it; 3 cite it directly.
0 of 27 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K011093: Agilent Information Center Software for M3150,M3151,M3153 and M3154, Agilent Technologies, Inc. (2001) Summary page 2.

## Most influential descendants
- K080192: Hypervisor VI Central Monitoring System (Including TMS) (2008), 20 descendants of its own
- K132036: Hypervisor Central Monitoring System (Including Telemetry Monitoring System, TMS-6016) (2014), 17 descendants of its own
- K150632: Hypervisor IX Monitoring System (2015), 14 descendants of its own
- K162607: BeneVision Central Monitoring System (2017), 12 descendants of its own
- K183238: BeneVision Central Monitoring System (2019), 11 descendants of its own

## Indications for use
The Central Monitoring System is intended to conduct centralized monitoring of adult, pediatric and neonatal vital sign information from multiple monitors in hospitals or medical institutions, the monitoring parameters include ECG, NIBP, SpO2, PR, RESP, IBP, TEMP, C02 and AG. It is not intended for home use.

Source page: https://510kreport.com/device/K062194
Methodology: https://510kreport.com/methodology