510(k) K934692 ยท MKJ Automated External Defibrillators (Non-Wearable)
K-DEFIB/PACE PEDIATRIC ELECTRODE
| Applicant | Katecho, Inc., Des Moines IA, US |
| Decision | Substantially Equivalent, Jan 24, 1995 |
| Received | Sep 30, 1993 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K934692
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.