510(k) K990762 ยท MKJ Automated External Defibrillators (Non-Wearable)
ZOLL M SERIES WITH RECTILINEAR BI-PHASIC OPTION (M SERIES BI-PHASIC)
| Applicant | Zoll Medical Corp, Burlington MA, US |
| Decision | Substantially Equivalent - Subject to Tracking Reg., Sep 3, 1999 |
| Received | Mar 8, 1999 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K990762
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.