ClearanceBrief
510(k) K770656 ยท DXY Implantable Pacemaker Pulse-Generator

GENERATOR, PULSE, CARDIAC 20U

ApplicantEdwards Pacemaker Systems, Mchenry IL, US
DecisionSubstantially Equivalent, Apr 26, 1977
ReceivedApr 7, 1977
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K770656

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.