510(k) K895662 ยท LDD Dc-Defibrillator, Low-Energy, (Including Paddles)
DEFIB K-PADS
| Applicant | Katecho, Inc., Des Moines IA, US |
| Decision | Substantially Equivalent, Jan 18, 1990 |
| Received | Sep 20, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K895662
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.