510(k) K911302 ยท DTD Pacemaker Lead Adaptor
MODELS 5866-24M/5866-38M/5866-40M/6986M ADAPT KIT
| Applicant | Medtronic Vascular, Minneapolis MN, US |
| Decision | Substantially Equivalent, Jul 30, 1991 |
| Received | Mar 25, 1991 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K911302
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.