510(k) K885204 ยท DSI Detector And Alarm, Arrhythmia
HORIZON 2000 ARRHYTHMIA MONITOR OPTION - (ALARMS)
| Applicant | Mennen Medical, Inc., Clarence NY, US |
| Decision | Substantially Equivalent, Apr 19, 1989 |
| Received | Dec 19, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K885204
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.