510(k) K913451 ยท DSI Detector And Alarm, Arrhythmia
HEWLETT-PACKARD MODEL 78720AC ARRHYTHMIA MONIT SYS
| Applicant | Hewlett-Packard Co., Waltham MA, US |
| Decision | Substantially Equivalent, Oct 31, 1991 |
| Received | Aug 2, 1991 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K913451
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.