510(k) K834416 ยท LDF Electrode, Pacemaker, Temporary
LUMELEC ELECTRODE CATHETER
| Applicant | Cordis Corp., Mchenry IL, US |
| Decision | Substantially Equivalent, Apr 24, 1984 |
| Received | Dec 15, 1983 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K834416
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.