510(k) K781252 ยท DXY Implantable Pacemaker Pulse-Generator
GENERATOR, PULSE, MODEL 5997
| Applicant | Medtronic Vascular, Walker MI, US |
| Decision | Substantially Equivalent, Oct 3, 1978 |
| Received | Jul 21, 1978 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K781252
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.