510(k) K874091 ยท LDD Dc-Defibrillator, Low-Energy, (Including Paddles)
360D DC DEFIBRILLATOR
| Applicant | Medac, Inc., Tualatin OR, US |
| Decision | Substantially Equivalent, Nov 23, 1987 |
| Received | Oct 7, 1987 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K874091
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.