# K000647: Datex-Ohmeda Network and Central

- Pathway: 510(k) (Traditional)
- Applicant: Datex-Ohmeda, Inc.
- Decided: Jul 13, 2000 after 136 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
No predicates in its family tree.
16 later devices descend from it; 2 cite it directly.
0 of 17 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
- K013246: Datex-Ohmeda S/5 Network and Central '01 (2001), 10 descendants of its own
- K022507: Datex-Ohmeda S/5 Network and Central '02 (2002), 9 descendants of its own
- K033281: Datex Ohmeda S/5 Network and Central (Icentral) '03 with L-NET03 Software (2003), 7 descendants of its own
- K042771: GE Datex-Ohmeda S/5 Network and Icentral '03, Sales Revision 3.3 (2004), 6 descendants of its own
- K052972: Datex-Ohmeda Network and Icentral '05, Sales Revision 4.3 (2005), 5 descendants of its own

Source page: https://510kreport.com/device/K000647
Methodology: https://510kreport.com/methodology
