510(k) K850968 ยท DTD Pacemaker Lead Adaptor
MEDTRONIC MODEL 4016 BIPOLAR ENDOCARDIAL SCREW-IN
| Applicant | Medtronic Vascular, Minneapolis MN, US |
| Decision | Substantially Equivalent, Aug 29, 1985 |
| Received | Mar 8, 1985 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K850968
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.