# K921014: Model M2350A and M2360A Wavevue Central Monitor

- Pathway: 510(k) (Traditional)
- Applicant: Hewlett-Packard Co.
- Decided: Oct 1, 1992 after 212 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.
4 later devices descend from it; 2 cite it directly.
0 of 5 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
- K070588: Philips Suresigns VSV (Vital Signs Viewer) (2007), 2 descendants of its own
- K131032: Philips Suresigns Central (2013), 1 descendant of its own
- K160951: Philips Efficia CMS200 Central Monitoring System (2016), 0 descendants of its own
- K970358: Ensemble Central Station Monitor (1998), 0 descendants of its own

Source page: https://510kreport.com/device/K921014
Methodology: https://510kreport.com/methodology