510(k) K060559 ยท MKJ Automated External Defibrillators (Non-Wearable)
ZOLL R SERIES DEFIBRILLATOR
| Applicant | ZOLL Medical Corporation, Chelsmford MA, US |
| Decision | Substantially Equivalent, Aug 17, 2006 |
| Received | Mar 2, 2006 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K060559
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Sep 29, 2009 | ZOLL Medical Corporation, World Wide Headquarters ZOLL R Series Defibrillator/Pacemaker/Monitor
Used by qualified medical personnel for the purpose of converting ventricular fibrillation to sinus rhythm or other cardiac rhythms capable of producing Terminated |
MKJ | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.