510(k) K964122 ยท DSI Detector And Alarm, Arrhythmia
HP STAR ST AND ARRHHYTHMIA SOFTWARE
| Applicant | Hewlett-Packard Co., Andover MA, US |
| Decision | Substantially Equivalent, Jan 8, 1997 |
| Received | Oct 15, 1996 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K964122
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.