510(k) K982025 ยท MKJ Automated External Defibrillators (Non-Wearable)
HEWLETT-PACKARD M2475B WITH 12-LEAD OPTION (#C90) CODEMASTER 100 CONITOR/DEFIBRILLATOR
| Applicant | Hewlett-Packard Co., Andover MA, US |
| Decision | Substantially Equivalent - Subject to Tracking Reg., Sep 4, 1998 |
| Received | Jun 9, 1998 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K982025
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.