510(k) K982220 ยท DTD Pacemaker Lead Adaptor
MODEL 2872 BIPOLAR LEAD ADAPTOR KIT
| Applicant | Medtronic Vascular, Minneapolis MN, US |
| Decision | Substantially Equivalent - Subject to Tracking Reg., Oct 15, 1998 |
| Received | Jun 24, 1998 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K982220
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.