510(k) K982264 ยท MKJ Automated External Defibrillators (Non-Wearable)
FIRSTSAVE BIPHASIC MODELS 9200 AND 9210
| Applicant | Survivalink Corp., Minnetonka MN, US |
| Decision | Substantially Equivalent - Subject to Tracking Reg., Jan 25, 1999 |
| Received | Jun 29, 1998 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K982264
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.