510(k) K800870 ยท DTB Permanent Pacemaker Electrode
MEDTRONIC MODEL 6958
| Applicant | Medtronic Vascular, Walker MI, US |
| Decision | Substantially Equivalent, Nov 13, 1980 |
| Received | Apr 17, 1980 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K800870
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.