# K012531: Datex-Ohmeda S/5 Device Interfacing Solution, N-Disxxxx

- Pathway: 510(k) (Traditional)
- Applicant: Datex-Ohmeda
- Decided: Nov 2, 2001 after 88 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: 1 generation back to K935477 (1994). 1 ancestor in all.
2 later devices descend 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)
- K935477: AS/3(TM) Anesthesia Monitor Syst Interface Board, Datex Division Instrumentarium Corp. (1994) Summary page 2.

## Most influential descendants
- K051634: Datex-Ohmeda S/5 Device Interfacing Solution (2005), 1 descendant of its own
- 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 is indicated for data transfer from ventilators/anesthesia machines, stand-alone monitors, blood gas analyzers and heartlung machines to Datex-Ohmeda bedside monitors for displaying and patient care information purposes. The devices are indicated for use by qualified medical personnel only.

Source page: https://510kreport.com/device/K012531
Methodology: https://510kreport.com/methodology