510(k) K070455 ยท MKJ Automated External Defibrillators (Non-Wearable)
ZOLL E SERIES WITH SEE-THRU CPR
| Applicant | Zoll Medical Corporation, World Wide Headquarters, Chelsmford MA, US |
| Decision | Substantially Equivalent, Apr 26, 2007 |
| Received | Feb 16, 2007 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K070455
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.