# K000168: CS/3 Critical Care Monitor with S-ICU99(a)

- Pathway: 510(k) (Traditional)
- Applicant: Datex-Ohmeda
- Decided: Apr 13, 2000 after 84 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.
2 later devices descend from it; 1 cites it directly.
0 of 3 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
- K021376: Datex-Ohmeda S/5 Critical Care Monitor with L-ICU02 and L-ICU02A Software (2002), 1 descendant of its own
- K071889: Datex-Ohmeda S/5 Critical Care Monitor with L-ICU05 and L-ICU05A Software (2008), 0 descendants of its own

Source page: https://510kreport.com/device/K000168
Methodology: https://510kreport.com/methodology