510(k) K853818 ยท LDF Electrode, Pacemaker, Temporary
MEDTRONIC MODEL 6405
| Applicant | Medtronic Vascular, Minneapolis MN, US |
| Decision | Substantially Equivalent, Oct 11, 1985 |
| Received | Sep 12, 1985 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K853818
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.