510(k) K892065 ยท MKJ Automated External Defibrillators (Non-Wearable)
LIFEPAK 250 DEFIBRILLATOR/MONITOR
| Applicant | Physio-Control Corp., Redmond WA, US |
| Decision | Substantially Equivalent, Jun 5, 1989 |
| Received | Mar 30, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K892065
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.