510(k) K780404 ยท DRT Monitor, Cardiac (Incl. Cardiotachometer & Rate Alarm)
ECG MONITORING SYSTEM,
| Applicant | Quinton, Inc. WA, US |
| Decision | Substantially Equivalent, Mar 28, 1978 |
| Received | Mar 13, 1978 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K780404
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.