510(k) K041892 ยท MKJ Automated External Defibrillators (Non-Wearable)
ZOLL AED PRO EXTERNAL DEFIBRILLATOR
| Applicant | ZOLL Medical Corporation, Chelsmford MA, US |
| Decision | Substantially Equivalent, Feb 4, 2005 |
| Received | Jul 13, 2004 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K041892
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.