510(k) K881810 ยท DTB Permanent Pacemaker Electrode
MEDTRONIC MODEL 4951P
| Applicant | Medtronic Vascular, Minneapolis MN, US |
| Decision | Substantially Equivalent, Oct 13, 1988 |
| Received | Apr 28, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K881810
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.