510(k) K924390 ยท LDF Electrode, Pacemaker, Temporary
ANGEMED 5000 LEAD ADAPTER
| Applicant | Angemed, Inc., Minneapolis MN, US |
| Decision | Substantially Equivalent, Aug 25, 1993 |
| Received | Aug 31, 1992 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K924390
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.