510(k) K011388 ยท MKJ Automated External Defibrillators (Non-Wearable)
ZOLL PAD
| Applicant | Zoll Medical Corp, Burlington MA, US |
| Decision | Substantially Equivalent, Mar 25, 2002 |
| Received | May 7, 2001 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K011388
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Feb 6, 2003 | Zoll Medical Corporation Zoll AED Plus Defibrillator (Automatic 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.