510(k) K940081 ยท DRT Monitor, Cardiac (Incl. Cardiotachometer & Rate Alarm)
MERCURY
| Applicant | Mennen Medical, Inc., Clarence NY, US |
| Decision | Substantially Equivalent, Apr 12, 1995 |
| Received | Jan 7, 1994 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K940081
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.