510(k) K073716 ยท MKJ Automated External Defibrillators (Non-Wearable)
LIFE+CEL OR LIFECEL BATTERY
| Applicant | Amco International Manufacturing & Design, Inc., Elizabeth CO, US |
| Decision | Substantially Equivalent, Apr 11, 2008 |
| Received | Dec 31, 2007 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K073716
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.