510(k) K944957 ยท LDF Electrode, Pacemaker, Temporary
TEMPORARY MYOCARDIAL PACING LEAD, MODEL 6500
| Applicant | Medtronic Blood Systems, Inc., Minneapolis MN, US |
| Decision | Substantially Equivalent, Jul 14, 1995 |
| Received | Oct 7, 1994 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K944957
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.