510(k) K883584 ยท MKJ Automated External Defibrillators (Non-Wearable)
FIRST MEDIC MODE 610
| Applicant | First Medical Devices Corp., Bellevue WA, US |
| Decision | Substantially Equivalent, Oct 6, 1988 |
| Received | Aug 22, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K883584
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.