510(k) K133269 ยท MKJ Automated External Defibrillators (Non-Wearable)
ZOLL X SERIES
| Applicant | Zoll Medical Corporation, World Wide Headquarters, Chelsmford MA, US |
| Decision | Substantially Equivalent, May 22, 2014 |
| Received | Oct 24, 2013 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K133269
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.