# K852514: Model 78560A Central Station Patient Info Sys

- Pathway: 510(k) (Traditional)
- Applicant: Hewlett-Packard Co.
- Decided: Sep 12, 1985 after 92 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
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
- K131032: Philips Suresigns Central (2013), 1 descendant of its own
- K160951: Philips Efficia CMS200 Central Monitoring System (2016), 0 descendants of its own

Source page: https://510kreport.com/device/K852514
Methodology: https://510kreport.com/methodology