510(k) K791093 ยท DXY Implantable Pacemaker Pulse-Generator
MODELS 2411/2418 VENTRICULAR-INHIBITED
| Applicant | Medtronic Vascular, Walker MI, US |
| Decision | Substantially Equivalent, Jun 20, 1979 |
| Received | Jun 12, 1979 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K791093
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.