510(k) K143714 ยท MKJ Automated External Defibrillators (Non-Wearable)
Powerheart G5 AED
| Applicant | Cardiac Science Corporation, Waukesha WI, US |
| Decision | Substantially Equivalent, May 4, 2015 |
| Received | Dec 29, 2014 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K143714
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.