510(k) K844103 ยท LDD Dc-Defibrillator, Low-Energy, (Including Paddles)
CARDIOPAC DEFIBRILLATOR 444
| Applicant | Birtcher Corp., El Monte CA, US |
| Decision | Substantially Equivalent, Jan 18, 1985 |
| Received | Oct 23, 1984 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K844103
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.