ClearanceBrief
510(k) K862226 ยท DXY Implantable Pacemaker Pulse-Generator

DIALOG MODELS 748, 748K AND 748T PULSE GENERATORS

ApplicantPacesetter Systems, Sylmar CA, US
DecisionSubstantially Equivalent, Feb 3, 1987
ReceivedJun 11, 1986
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K862226

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.