510(k) K832561 ยท LDF Electrode, Pacemaker, Temporary
EPCOR MULTIELECTRODE TEMP. PERVENOUS
| Applicant | Cordis Corp., Mchenry IL, US |
| Decision | Substantially Equivalent, Oct 19, 1983 |
| Received | Aug 1, 1983 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K832561
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.