510(k) K092391 ยท MKJ Automated External Defibrillators (Non-Wearable)
MOBILEAED, MOBILEALS, MOBILEAED+ AND ADVANTAGEAED
| Applicant | Concord Medical Products, Burlington MA, US |
| Decision | Substantially Equivalent, Apr 1, 2010 |
| Received | Aug 5, 2009 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K092391
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.