510(k) K864640 ยท DTB Permanent Pacemaker Electrode
ANCOR PERVENOUS ACTIVE FIXATION UNIPOLAR LEAD
| Applicant | Cordis Corp., Miami FL, US |
| Decision | Substantially Equivalent, Jan 6, 1987 |
| Received | Nov 26, 1986 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K864640
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.