510(k) K832422 ยท DTB Permanent Pacemaker Electrode
CORDIS ANCOR ACTIVE FIXATION LEAD
| Applicant | Cordis Corp., Miami FL, US |
| Decision | Substantially Equivalent, Aug 5, 1986 |
| Received | Jul 22, 1983 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K832422
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.