510(k) K811318 ยท LDF Electrode, Pacemaker, Temporary
TEMPORARY ENDOCARDIAL TRIPOLAR LD. #6880
| Applicant | Medtronic Vascular, Walker MI, US |
| Decision | Substantially Equivalent, Jul 20, 1981 |
| Received | May 12, 1981 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K811318
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.