510(k) K091561 ยท MKJ Automated External Defibrillators (Non-Wearable)
ZOLL AED PLUS VERSION 5.32 SOFTWARE RELEASE
| Applicant | ZOLL Medical Corporation, Chelsmford MA, US |
| Decision | Substantially Equivalent, Sep 23, 2010 |
| Received | May 28, 2009 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K091561
No recall in the FDA data names this 510(k).
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.