510(k) K811123 ยท DXY Implantable Pacemaker Pulse-Generator
MEDTRONIC PULSE GENERATOR
| Applicant | Medtronic Vascular, Walker MI, US |
| Decision | Substantially Equivalent, May 27, 1981 |
| Received | Apr 24, 1981 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K811123
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.