510(k) K810755 ยท DRT Monitor, Cardiac (Incl. Cardiotachometer & Rate Alarm)
SQUINN VITATEK 500 SERIES PHYSIOL. MONI
| Applicant | Vitatek, Walker MI, US |
| Decision | Substantially Equivalent, Apr 3, 1981 |
| Received | Mar 20, 1981 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K810755
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.