510(k) K072812 ยท MKJ Automated External Defibrillators (Non-Wearable)
PHILIPS HEARTSTART SMARTPADS III
| Applicant | Philips Medical Systems, Seattle WA, US |
| Decision | Substantially Equivalent, Feb 26, 2008 |
| Received | Oct 1, 2007 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K072812
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.