510(k) K811259 ยท DTB Permanent Pacemaker Electrode
CORDIS ENCOR ATRIAL LEAD
| Applicant | Cordis Corp., Walker MI, US |
| Decision | Substantially Equivalent, Dec 27, 1984 |
| Received | May 6, 1981 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K811259
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.