ClearanceBrief
510(k) K850464 ยท DXY Implantable Pacemaker Pulse-Generator

PROGRAMALITH III 240 PULSE GENERATOR

ApplicantPacesetter Systems, Sylmar CA, US
DecisionSubstantially Equivalent, May 15, 1985
ReceivedFeb 7, 1985
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K850464

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.