510(k) K831645 ยท LDF Electrode, Pacemaker, Temporary
TEMP. BIPOLAR EPICARDIAL LEAD
| Applicant | Cordic Corp., Mchenry IL, US |
| Decision | Substantially Equivalent, Jul 26, 1983 |
| Received | May 23, 1983 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K831645
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.