510(k) K110361 ยท MKJ Automated External Defibrillators (Non-Wearable)
ZOLL R SERIES WITH 2010 AHA GUIDELINES SOFTWARE UPDATE
| Applicant | Zoll Medical Corporation, World Wide Headquarters, Chelsmford MA, US |
| Decision | Substantially Equivalent, Mar 8, 2011 |
| Received | Feb 7, 2011 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K110361
No recall in the FDA data names this 510(k).
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