510(k) K010257 ยท MKJ Automated External Defibrillators (Non-Wearable)
ZOLL M SERIES
| Applicant | Zoll Medical Corp, Burlington MA, US |
| Decision | Substantially Equivalent, Feb 28, 2001 |
| Received | Jan 29, 2001 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K010257
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Sep 17, 2004 | Zoll Medical Corporation Zoll M Series Automated Defibrillator (AED) Terminated |
MKT | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.