510(k) K810432 ยท DTB Permanent Pacemaker Electrode
CORDIS PERVENOUS ATRIAL LEAD
| Applicant | Cordis Corp., Mchenry IL, US |
| Decision | Substantially Equivalent, Mar 13, 1981 |
| Received | Feb 19, 1981 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K810432
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.