# K000882: Datex-Ohmeda CS/3 Telemetry System

- Pathway: 510(k) (Traditional)
- Applicant: Datex-Ohmeda
- Decided: Jun 5, 2000 after 77 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
No predicates in its family tree.
11 later devices descend from it; 1 cites it directly.
0 of 12 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA has not posted a summary or statement for it, so its predicates are not known.

## Most influential descendants
- K060135: Mortara Surveyor Telemetry Central Station (2006), 10 descendants of its own
- K131929: Surveyor Central Station (2013), 6 descendants of its own
- K133973: Tempus Pro with Enhanced Features (2014), 3 descendants of its own
- K170567: Tempus Pro Patient Monitor (2017), 2 descendants of its own
- K123556: Mortara Surveyor Patient Monitor (2013), 2 descendants of its own

Source page: https://510kreport.com/device/K000882
Methodology: https://510kreport.com/methodology