510(k) K780809 ยท DXY Implantable Pacemaker Pulse-Generator
GENERATOR, PULSE MODELS 5920/5921
| Applicant | Medtronic Vascular, Walker MI, US |
| Decision | Substantially Equivalent, Jul 28, 1978 |
| Received | May 18, 1978 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K780809
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.