510(k) K033474 ยท MKJ Automated External Defibrillators (Non-Wearable)
ZOLL AED PLUS
| Applicant | Zoll Medical Corp, Chelsmford MA, US |
| Decision | Substantially Equivalent, May 21, 2004 |
| Received | Nov 3, 2003 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K033474
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Apr 1, 2009 | ZOLL Medical Corporation, World Wide Headquarters Zoll AED Plus Defibrillator Terminated |
MKJ | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.