510(k) K896903 ยท LDD Dc-Defibrillator, Low-Energy, (Including Paddles)
FIRST MEDIC MODEL 510
| Applicant | Spacelabs, Inc., Redmond WA, US |
| Decision | Substantially Equivalent, Dec 27, 1990 |
| Received | Dec 8, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K896903
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.