# K961165: HP M2600A Omnicare Telemetry System Model M2600A

- Pathway: 510(k) (Traditional)
- Applicant: Hewlett-Packard Co.
- Decided: Oct 10, 1996 after 199 days
- Product code: DSI (Detector And Alarm, Arrhythmia)
- 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 K894277 (1989). 1 ancestor in all.
27 later devices descend from it; 1 cites it directly.
0 of 29 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K894277: M1400A Transmitter,M1402 Receiver,M1401 Mainframe, Hewlett-Packard Co. (1989) Summary page 1.

## Most influential descendants
- K983996: Spacelabs Medical Ultraview Digital Telemtry System (1999), 26 descendants of its own
- 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

## Indications for use
The device is intended to provide ambulatory and nonambulatory monitoring of ECG and SpO, parameters of adult, and pediatric patients in a professional health care facility. It is intended to be used by trained health care personnel. It is not intended for home use.

Source page: https://510kreport.com/device/K961165
Methodology: https://510kreport.com/methodology