# K052880: Datex-Ohmeda S/5 Interface Module E-Int

- Pathway: 510(k) (Special)
- Applicant: GE Healthcare
- Decided: Nov 2, 2005 after 21 days
- Product code: CCK (Analyzer, Gas, Carbon-Dioxide, Gaseous-Phase)
- Device class: 2
- Regulation: 21 CFR 868.1400
- 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.
No later device cites it as a predicate yet.
0 of 2 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 1.

## Indications for use
The Datex-Ohmeda S/5 T E-INT module is indicated for integration of external measurement devices to the Datex-Ohmeda S/5 Monitors. The device is indicated for use by qualified medical personnel only.

Source page: https://510kreport.com/device/K052880
Methodology: https://510kreport.com/methodology