510(k) K851064 ยท DTB Permanent Pacemaker Electrode
CORDIS HI-FLEX PERVENOUS ACTIVE FIXATION UNIPOLAR
| Applicant | Cordis Corp., Miami FL, US |
| Decision | Substantially Equivalent, Aug 5, 1986 |
| Received | Mar 15, 1985 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K851064
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.