510(k) K991007 ยท MKJ Automated External Defibrillators (Non-Wearable)
K-DEFIB/PACE RADIOLUCENT ADULT ELECTRODE, MODEL KRT-60
| Applicant | Katecho, Inc., Des Moines IA, US |
| Decision | Substantially Equivalent, Aug 23, 1999 |
| Received | Mar 26, 1999 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K991007
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.