510(k) K991871 ยท MKJ Automated External Defibrillators (Non-Wearable)
HEWLETT PACKARD MULTI FUNCTION ADULT DEFIB ELECTRODE, MODEL M3501A & M3502A
| Applicant | Hewlett-Packard Co., Des Moines IA, US |
| Decision | Substantially Equivalent, Aug 5, 1999 |
| Received | Jun 1, 1999 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K991871
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.