510(k) K895009 ยท LDD Dc-Defibrillator, Low-Energy, (Including Paddles)
GEL-TAC(R)
| Applicant | Padeco, Inc., Lake Oswego OR, US |
| Decision | Substantially Equivalent, Dec 13, 1989 |
| Received | Aug 8, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K895009
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.