510(k) K760160 ยท DRT Monitor, Cardiac (Incl. Cardiotachometer & Rate Alarm)
MONITOR, PATIENT (MODEL 78333A)
| Applicant | Hewlett-Packard Co., Mchenry IL, US |
| Decision | Substantially Equivalent, Jul 19, 1976 |
| Received | Jul 2, 1976 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K760160
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.