510(k) K801284 ยท DTB Permanent Pacemaker Electrode
LOW PROFILE LEAD CONNECTOR MODIFICATION (4002)
| Applicant | Medtronic Vascular, Minneapolis MN, US |
| Decision | Substantially Equivalent, Dec 1, 1980 |
| Received | May 29, 1980 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K801284
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.