510(k) K854582 ยท DTB Permanent Pacemaker Electrode
MOD TARGET/TIPS # 4011,4012,4511,4512,6912,4016
| Applicant | Medtronic Vascular, Minneapolis MN, US |
| Decision | Substantially Equivalent, Jan 13, 1986 |
| Received | Nov 15, 1985 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K854582
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.