510(k) K760671 ยท DXY Implantable Pacemaker Pulse-Generator
PACEMAKERS, VITATRONS (SERIES 3000)
| Applicant | Vitatron Medical BV, Mchenry IL, US |
| Decision | Substantially Equivalent, Nov 12, 1976 |
| Received | Sep 17, 1976 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K760671
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.