510(k) K110526 ยท MKJ Automated External Defibrillators (Non-Wearable)
ZOLL AEDPRO WITH 2010 AHA GUIDELINES SOFTWARE UPDATE
| Applicant | ZOLL Medical Corporation, Chelsmford MA, US |
| Decision | Substantially Equivalent, Mar 25, 2011 |
| Received | Feb 24, 2011 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K110526
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.