510(k) K780937 ยท DRT Monitor, Cardiac (Incl. Cardiotachometer & Rate Alarm)
MODEL 20 DIGITAL PULSE RATE MONITOR
| Applicant | Sentronix, Inc., Mchenry IL, US |
| Decision | Substantially Equivalent, Aug 31, 1978 |
| Received | Jun 8, 1978 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K780937
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.