510(k) K812725 ยท LDF Electrode, Pacemaker, Temporary
MODEL 5867-12 BIPOLAR LOW-PROFILE LEAD
| Applicant | Medtronic Vascular, Walker MI, US |
| Decision | Substantially Equivalent, Nov 16, 1981 |
| Received | Sep 28, 1981 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K812725
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.