510(k) K110168 ยท MKJ Automated External Defibrillators (Non-Wearable)
ZOLL E SERIES WITH 2010 AHA GUIDLINES SOFTWARE UPDATE
| Applicant | Zoll Medical Corporation, World Wide Headquarters, Chelsmford MA, US |
| Decision | Substantially Equivalent, Feb 17, 2011 |
| Received | Jan 20, 2011 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K110168
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.