510(k) K802259 ยท LDF Electrode, Pacemaker, Temporary
TRANSVENOUS PACEMAKER ELECTRODE KIT
| Applicant | Stanco Medical, Inc., Mchenry IL, US |
| Decision | Substantially Equivalent, Oct 23, 1980 |
| Received | Sep 16, 1980 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K802259
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.