510(k) K854307 ยท LDD Dc-Defibrillator, Low-Energy, (Including Paddles)
KONTRON DEFIBRILLATOR 7501
| Applicant | Kontron Instruments, Inc., Everett MA, US |
| Decision | Substantially Equivalent, Dec 4, 1985 |
| Received | Oct 25, 1985 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K854307
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.