510(k) K790292 ยท DRT Monitor, Cardiac (Incl. Cardiotachometer & Rate Alarm)
MONITOR, ELECTROCARDIOSCOPE
| Applicant | Burdick Corp., Mchenry IL, US |
| Decision | Substantially Equivalent, Feb 26, 1979 |
| Received | Feb 9, 1979 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K790292
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.