510(k) K992323 ยท MLD Monitor, St Segment With Alarm
DATEX-OHMEDA CARDIOCAP 5, F-MX, F-MXG AND ACCESSORIES
| Applicant | Datex-Ohmeda, Inc., Tewksburt MA, US |
| Decision | Substantially Equivalent, Nov 1, 1999 |
| Received | Jul 12, 1999 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K992323
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Jul 20, 2004 | Datex-Ohmeda Inc Datex-Ohmeda Cardiocap/5 Patient Monitors Terminated |
MHX | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.