510(k) K031210 ยท DTB Permanent Pacemaker Electrode
MODEL 4951M MYOCARDIAL UNIPOLAR LEAD
| Applicant | Metronic, Inc., Minneapolis MN, US |
| Decision | Substantially Equivalent, May 16, 2003 |
| Received | Apr 17, 2003 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K031210
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.