ClearanceBrief
510(k) K861140 ยท DXY Implantable Pacemaker Pulse-Generator

PROGRAMALITH III PULSE GENERATOR

ApplicantPacesetter Systems, Sylmar CA, US
DecisionSubstantially Equivalent, May 2, 1986
ReceivedMar 26, 1986
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K861140

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.