510(k) K895789 ยท LDF Electrode, Pacemaker, Temporary
UNIPOLAR TEMP. MYOCARDIAL HEART WIRE, MODEL 6490
| Applicant | Medtronic Vascular, Minneapolis MN, US |
| Decision | Substantially Equivalent, Dec 7, 1989 |
| Received | Sep 28, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K895789
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.