510(k) K964832 ยท DSI Detector And Alarm, Arrhythmia
HEWLETT-PACKARD CENTRALVUE SOFTWARE
| Applicant | Hewlett-Packard Co., Andover MA, US |
| Decision | Substantially Equivalent, May 15, 1997 |
| Received | Dec 2, 1996 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K964832
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.