510(k) K923747 ยท DSI Detector And Alarm, Arrhythmia
CC ARHYTHMIS MONITORING OPTION
| Applicant | Hewlett-Packard Co., Waltham MA, US |
| Decision | Substantially Equivalent, Jul 20, 1993 |
| Received | Jul 9, 1992 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K923747
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.