510(k) K910870 ยท DRT Monitor, Cardiac (Incl. Cardiotachometer & Rate Alarm)
EDENTEC MODEL 3711 DIGITAL RECORDER
| Applicant | Edentec Corp., Eden Prairie MN, US |
| Decision | Substantially Equivalent, Aug 29, 1991 |
| Received | Mar 1, 1991 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K910870
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.