510(k) K760803 ยท DRT Monitor, Cardiac (Incl. Cardiotachometer & Rate Alarm)
PHYSIOLOGICAL MONITOR (MODEL 870)
| Applicant | Datascope Corp., Mchenry IL, US |
| Decision | Substantially Equivalent, Oct 20, 1976 |
| Received | Oct 12, 1976 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K760803
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.