510(k) K972241 ยท MKJ Automated External Defibrillators (Non-Wearable)
ZOLL REVIVER
| Applicant | Zoll Medical Corp, Burlington MA, US |
| Decision | Substantially Equivalent, Mar 16, 1998 |
| Received | Jun 16, 1997 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K972241
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Jul 10, 2003 | Zoll Medical Corporation Zoll M Series External Defibrillator Terminated |
MKJ | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.