510(k) K770239 ยท DRT Monitor, Cardiac (Incl. Cardiotachometer & Rate Alarm)
DIGITAL HEART RATE METER
| Applicant | Burdick Corp., Mchenry IL, US |
| Decision | Substantially Equivalent, Feb 14, 1977 |
| Received | Feb 7, 1977 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K770239
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.