510(k) K130153 ยท MKJ Automated External Defibrillators (Non-Wearable)
HEARSTART MRX WITH AIRWAY CONFIMRATION ASSIST
| Applicant | Philips Medical Systems, Andover MA, US |
| Decision | Substantially Equivalent, Mar 12, 2013 |
| Received | Jan 22, 2013 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K130153
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.