510(k) K894976 ยท DTD Pacemaker Lead Adaptor
ALTERNATE PACKAGING CONF. OF PACEMAKER LEAD ADAP.
| Applicant | Medtronic Vascular, Minneapolis MN, US |
| Decision | Substantially Equivalent, Oct 12, 1989 |
| Received | Aug 7, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K894976
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.