510(k) K140972 ยท LDF Electrode, Pacemaker, Temporary
UNIPOLAR PEDIATRIC TEMPORARY PACING LEAD, UNIPOLAR TEMPORARY ATRIAL PACING LEAD, UNIPOLAR TEMPORARY MYOCARDIAL PACING
| Applicant | Medtronic, Inc., Santa Ana CA, US |
| Decision | Substantially Equivalent, Jun 6, 2014 |
| Received | Apr 16, 2014 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K140972
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.