510(k) K954809 ยท LDF Electrode, Pacemaker, Temporary
UNIPOLAR TEMPORARY MYOCARDIAL PACING WIRE MODEL 6494
| Applicant | Medtronic Vascular, Minneapolis MN, US |
| Decision | Substantially Equivalent, Dec 13, 1995 |
| Received | Oct 19, 1995 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K954809
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.