510(k) K012460 ยท LDF Electrode, Pacemaker, Temporary
MODEL 6495 BIPOLAR TEMPORARY MYOCARDIAL PACING LEAD
| Applicant | Medtronic Vascular, Minneapolis MN, US |
| Decision | Substantially Equivalent, Aug 14, 2001 |
| Received | Aug 1, 2001 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K012460
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.