510(k) K900627 ยท DTD Pacemaker Lead Adaptor
MODEL 5866-34 LEAD ADAPTOR KIT
| Applicant | Medtronic Vascular, Minneapolis MN, US |
| Decision | Substantially Equivalent, Apr 20, 1990 |
| Received | Feb 8, 1990 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K900627
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.