510(k) K953204 ยท MKJ Automated External Defibrillators (Non-Wearable)
PEDIATRIC QUIK-COMBO
| Applicant | Physio-Control Corp., Redmond WA, US |
| Decision | Substantially Equivalent, Jan 11, 1996 |
| Received | Jul 6, 1995 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K953204
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.