510(k) K051475 ยท MKJ Automated External Defibrillators (Non-Wearable)
ZOLL M SERIES 12SL ANALYSIS OPTION
| Applicant | ZOLL Medical Corporation, Chelsmford MA, US |
| Decision | Substantially Equivalent, Jun 24, 2005 |
| Received | Jun 3, 2005 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K051475
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.