510(k) K081081 ยท MKJ Automated External Defibrillators (Non-Wearable)
ZOLL E SERIES WITH BLUETOOTH DIAL UP NETWORKING
| Applicant | Zoll Medical Corporation, World Wide Headquarters, Chelsmford MA, US |
| Decision | Substantially Equivalent, Mar 9, 2009 |
| Received | Apr 16, 2008 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K081081
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.