510(k) K000882 ยท MHX Monitor, Physiological, Patient(With Arrhythmia Detection Or Alarms)
DATEX-OHMEDA CS/3 TELEMETRY SYSTEM
| Applicant | Datex-Ohmeda, Tewksbury MA, US |
| Decision | Substantially Equivalent, Jun 5, 2000 |
| Received | Mar 20, 2000 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K000882
No recall in the FDA data names this 510(k).
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.