510(k) K935083 ยท LDD Dc-Defibrillator, Low-Energy, (Including Paddles)
PEDIATRIC DEFIB K-PADS
| Applicant | Katecho, Inc., Des Moines IA, US |
| Decision | Substantially Equivalent - Subject to Tracking Reg., Jul 25, 1994 |
| Received | Oct 25, 1993 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K935083
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.