510(k) K133239 ยท MKJ Automated External Defibrillators (Non-Wearable)
ZOLL E SERIES
| Applicant | Zoll Medical Corporation, World Wide Headquarters, Chelsmford MA, US |
| Decision | Substantially Equivalent, Jan 16, 2015 |
| Received | Oct 21, 2013 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K133239
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.