ClearanceBrief
510(k) K872779 ยท DXY Implantable Pacemaker Pulse-Generator

PROLOG MP PULSE GENERATORS 658K AND 658T

ApplicantPacesetter Systems, Sylmar CA, US
DecisionSubstantially Equivalent, Nov 4, 1987
ReceivedJul 14, 1987
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K872779

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.