510(k) K863899 ยท LDD Dc-Defibrillator, Low-Energy, (Including Paddles)
K-STIK DEFIBRILLATION PADS
| Applicant | Katecho, Inc., Des Moines IA, US |
| Decision | Substantially Equivalent, Nov 12, 1986 |
| Received | Oct 7, 1986 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K863899
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.