510(k) K954085 ยท DTB Permanent Pacemaker Electrode
MODELS 5866-45 AND 5866-46 SIZING SLEEVE
| Applicant | Medtronic Vascular, Minneapolis MN, US |
| Decision | Substantially Equivalent - Subject to Tracking Reg., Nov 7, 1995 |
| Received | Aug 28, 1995 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K954085
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.