510(k) K032439 ยท MKJ Automated External Defibrillators (Non-Wearable)
ZOLL M SERIES WITH RECTILINEAR BI-PHASIC OPTION (M SERIES BI-PHASIC)
| Applicant | Zoll Medical Corp, Chelsmford MA, US |
| Decision | Substantially Equivalent, Nov 5, 2003 |
| Received | Aug 7, 2003 |
| Type | Abbreviated |
| FDA record | Open on fda.gov |
Recalls that name K032439
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.