510(k) K971910 ยท DSI Detector And Alarm, Arrhythmia
MULTI-PARAMETER MODULE (M3000A)/DISPLAY UNIT (M3046A)
| Applicant | Hewlett-Packard GmbH, Wuerttemberg, DE |
| Decision | Substantially Equivalent, Mar 23, 1998 |
| Received | May 23, 1997 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K971910
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.