510(k) K863404 ยท LDD Dc-Defibrillator, Low-Energy, (Including Paddles)
CARDIOLIFE TEC 7100
| Applicant | Nihon Kohden America, Inc., Irvine CA, US |
| Decision | Substantially Equivalent, Oct 31, 1986 |
| Received | Sep 3, 1986 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K863404
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.