510(k) K052316 ยท MKJ Automated External Defibrillators (Non-Wearable)
POWERHEART ECD
| Applicant | Cardiac Science, Inc., Edina MN, US |
| Decision | Substantially Equivalent, Jan 3, 2006 |
| Received | Aug 25, 2005 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K052316
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.