# K151366: Philips CS770 IntelliSpace Critical Care and Anesthesia

- Pathway: 510(k) (Traditional)
- Applicant: Philips Medical Systems
- Decided: Oct 30, 2015 after 162 days
- Product code: DXJ (Display, Cathode-Ray Tube, Medical)
- Device class: 2
- Regulation: 21 CFR 870.2450
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 6 generations back to K941811 (1994). 16 ancestors in all.
No later device cites it as a predicate yet.
0 of 17 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K100272: Intellivue Clinical Information Portfolio, Philips Medical Systems (2010) Summary page 6.

## Indications for use
Intended for use in the data collection, storage, and management with independent bedside devices, and ancillary systems that are connected either directly or through networks. The device is indicated for use whenever there is a need for generation of a patient record and computation of drug dosage in all areas patient care is given in the hospital, including critical care and anesthesia areas.

Source page: https://510kreport.com/device/K151366
Methodology: https://510kreport.com/methodology