510(k) K103567 ยท MKJ Automated External Defibrillators (Non-Wearable)
LIFEPAK 15 MONITOR/DEFIBRILLATOR
| Applicant | Physio-Control, Inc., Redmond WA, US |
| Decision | Substantially Equivalent, Mar 22, 2011 |
| Received | Dec 6, 2010 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K103567
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.