ClearanceBrief
510(k) K760669 ยท DXY Implantable Pacemaker Pulse-Generator

PACEMAKERS, VITATRON'S

ApplicantVitatron Medical BV, Mchenry IL, US
DecisionSubstantially Equivalent, Nov 12, 1976
ReceivedSep 17, 1976
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K760669

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.