510(k) K992977 ยท MKJ Automated External Defibrillators (Non-Wearable)
HEWLETT PACKARD MULTIFUNCTION PEDIATRIC DEFIB FUNCTION, MODEL M3503A & M3504A
| Applicant | Hewlett-Packard Co., Des Moines IA, US |
| Decision | Substantially Equivalent, Dec 1, 1999 |
| Received | Sep 3, 1999 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K992977
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.