510(k) K122758 ยท MKJ Automated External Defibrillators (Non-Wearable)
POWERHEART G5 AED
| Applicant | Cardiac Science Corporation, Waukesha WI, US |
| Decision | Substantially Equivalent, Feb 12, 2014 |
| Received | Sep 10, 2012 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K122758
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.