510(k) K982992 ยท MKJ Automated External Defibrillators (Non-Wearable)
ZOLL M SERIES SPO2 OPTION
| Applicant | Zoll Medical Corp, Burlington MA, US |
| Decision | Substantially Equivalent - Subject to Tracking Reg., Mar 11, 1999 |
| Received | Aug 27, 1998 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K982992
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.