510(k) K791920 ยท DXY Implantable Pacemaker Pulse-Generator
CARDIAC PACEMAKER P4000 SER. & P1000
| Applicant | Vitatron Medical BV, Mchenry IL, US |
| Decision | Substantially Equivalent, Nov 29, 1979 |
| Received | Sep 25, 1979 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K791920
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.