510(k) K881273 ยท DSI Detector And Alarm, Arrhythmia
HORIZON 2000 ARRHYTHMIA MONITORING OPTION
| Applicant | Mennen Medical, Inc., Clarence NY, US |
| Decision | Substantially Equivalent, Jul 12, 1988 |
| Received | Mar 25, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K881273
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.