# K051634: Datex-Ohmeda S/5 Device Interfacing Solution

- Pathway: 510(k) (Special)
- Applicant: GE Healthcare
- Decided: Jul 19, 2005 after 29 days
- Product code: MSX (System, Network And Communication, Physiological Monitors)
- Device class: 2
- Regulation: 21 CFR 870.2300
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 2 generations back to K935477 (1994). 2 ancestors in all.
1 later device descends from it; 1 cites it directly.
0 of 4 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K012531: Datex-Ohmeda S/5 Device Interfacing Solution, N-Disxxxx, Datex-Ohmeda (2001) Summary page 1.

## Most influential descendants
- K070421: Datex-Ohmeda S/5 Device Interfacing Solution, N-Disxxxx..01 with N-Disvent..02 (2007), 0 descendants of its own

## Indications for use
The Datex-Ohmeda S/5 Device Interfacing Solution, N-DISxxxx..01, is indicated for data transfer between stand-alone monitors, ventilators/anesthesia machines, blood gas analyzers, and heart-lung machines and Datex-Ohmeda bedside monitors for displaying and patient care information purposes. The device is indicated for use by qualified medical personnel only.

Source page: https://510kreport.com/device/K051634
Methodology: https://510kreport.com/methodology