510(k) K981376 ยท DSI Detector And Alarm, Arrhythmia
HEWLETT-PACKARD M1205A VIRIDIA 24 CT
| Applicant | Hewlett-Packard Co., Andover MA, US |
| Decision | Substantially Equivalent, Jan 4, 1999 |
| Received | Apr 16, 1998 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K981376
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.