510(k) K910630 ยท DTD Pacemaker Lead Adaptor
MODEL 6985M TEMPORARY UNIPOLAR LEAD EXTENDER KIT
| Applicant | Medtronic Vascular, Minneapolis MN, US |
| Decision | Substantially Equivalent, Apr 18, 1991 |
| Received | Feb 13, 1991 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K910630
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.