510(k) K963898 ยท LDF Electrode, Pacemaker, Temporary
MODEL 6495 BIPOLAR TEMPORARY PACING LEAD
| Applicant | Medtronic Vascular, Minneapolis MN, US |
| Decision | Substantially Equivalent, Jul 22, 1997 |
| Received | Sep 27, 1996 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K963898
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Apr 14, 2009 | Medtronic Inc Medtronic STREAMLINE Bipolar Temporary Myocardial Pacing Lead, 6495, Sterile EO, REF 6495F, Medtronic, INC., Minneapolis, MN 55432 Terminated |
LDF | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.