510(k) K915724 ยท DTD Pacemaker Lead Adaptor
MODEL 6984M LEAD EXTENDER KIT
| Applicant | Medtronic Vascular, Minneapolis MN, US |
| Decision | Substantially Equivalent, Feb 18, 1992 |
| Received | Dec 20, 1991 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K915724
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.