510(k) K071025 ยท MKJ Automated External Defibrillators (Non-Wearable)
ZOLL AEDPRO WITH SEE-THRU CPR, MODEL AEDPRO
| Applicant | Zoll Medical Corporation, World Wide Headquarters, Chelsmford MA, US |
| Decision | Substantially Equivalent, Jun 22, 2007 |
| Received | Apr 11, 2007 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K071025
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.