510(k) K810041 ยท LDF Electrode, Pacemaker, Temporary
CORDIS TEMPORATY CURVED ATRIAL LEAD
| Applicant | Cordis Corp. MD, US |
| Decision | Substantially Equivalent, Feb 5, 1981 |
| Received | Jan 7, 1981 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K810041
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.