510(k) K940445 ยท MKJ Automated External Defibrillators (Non-Wearable)
VIVALINK AED DEFIBRILLATOR
| Applicant | Survivalink Corp., Minnetonka MN, US |
| Decision | Substantially Equivalent, Feb 9, 1995 |
| Received | Feb 1, 1994 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K940445
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.