510(k) K962036 ยท DTB Permanent Pacemaker Electrode
MEDTRONIC MODEL 5058 BIPOLAR, IMPLANTABLE, SCREW-IN, VENTRICULAR/ATRIAL, TRANSVENOUS LEAD
| Applicant | Medtronic Vascular, Minneapolis MN, US |
| Decision | Substantially Equivalent - Subject to Tracking Reg., Aug 22, 1996 |
| Received | May 24, 1996 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K962036
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.