510(k) K892005 ยท MKJ Automated External Defibrillators (Non-Wearable)
SHOCK ADVISORY ADAPTER FOR USE W/LIFEPAK 9
| Applicant | Physio-Control Corp., Redmond WA, US |
| Decision | Substantially Equivalent, Jun 20, 1989 |
| Received | Mar 28, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K892005
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.