510(k) K892066 ยท DRT Monitor, Cardiac (Incl. Cardiotachometer & Rate Alarm)
HORIZON CENTRAL STATION
| Applicant | Mennen Medical, Inc., Clarence NY, US |
| Decision | Substantially Equivalent, Jun 22, 1989 |
| Received | Mar 30, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K892066
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.