510(k) K900982 ยท LDF Electrode, Pacemaker, Temporary
E-CLIP
| Applicant | Joel Cohen & Esther R. Cohen, Plantation FL, US |
| Decision | Substantially Equivalent, Apr 19, 1990 |
| Received | Mar 2, 1990 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K900982
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.