510(k) K993745 ยท MKJ Automated External Defibrillators (Non-Wearable)
K-DEFIB/PACE ADULT ELECTRODE, MODEL KDP-80
| Applicant | Katecho, Inc., Des Moines IA, US |
| Decision | Substantially Equivalent, Feb 3, 2000 |
| Received | Nov 5, 1999 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K993745
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.