510(k) K812781 ยท LDF Electrode, Pacemaker, Temporary
TEMPORARY PERVENOUS J-ATRIAL LEAD
| Applicant | Cordis Corp., Mchenry IL, US |
| Decision | Substantially Equivalent, Oct 29, 1981 |
| Received | Oct 5, 1981 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K812781
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.