510(k) K903919 ยท DXY Implantable Pacemaker Pulse-Generator
IMPLANTABLE PULSE DEVICES
| Applicant | Medtronic Vascular, Minneapolis MN, US |
| Decision | Substantially Equivalent, Oct 23, 1990 |
| Received | Aug 24, 1990 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K903919
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.