510(k) K864856 ยท DTB Permanent Pacemaker Electrode
MODEL 5866-24 PACEMAKER LEAD ADAPTOR
| Applicant | Medtronic Vascular, Minneapolis MN, US |
| Decision | Substantially Equivalent, Jan 6, 1987 |
| Received | Dec 11, 1986 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K864856
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.