510(k) K991556 ยท MKJ Automated External Defibrillators (Non-Wearable)
ZOLL M SERIES 12SL ANALYSIS OPTION
| Applicant | Zoll Medical Corp, Burlington MA, US |
| Decision | Substantially Equivalent - Subject to Tracking Reg., Oct 21, 1999 |
| Received | May 4, 1999 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K991556
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.