510(k) K850880 ยท DRT Monitor, Cardiac (Incl. Cardiotachometer & Rate Alarm)
HORIZON 1000 CARDIAC MONITOR
| Applicant | Mennen Medical, Inc., Clarence NY, US |
| Decision | Substantially Equivalent, Apr 25, 1985 |
| Received | Mar 4, 1985 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K850880
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.