510(k) K922182 ยท LDF Electrode, Pacemaker, Temporary
UNIPOLAR ATRIAL TEMPORARY PACING LEAD, MODEL 6492
| Applicant | Medtronic Vascular, Minneapolis MN, US |
| Decision | Substantially Equivalent, Nov 23, 1992 |
| Received | May 11, 1992 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K922182
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.