ClearanceBrief
510(k) K853400 ยท DXY Implantable Pacemaker Pulse-Generator

CCS IMPLANTABLE MAESTRO SERIES 200 CARDIAC PACEMAK

ApplicantCardiac Control Systems, Inc., Palm Coast FL, US
DecisionSubstantially Equivalent, Feb 24, 1986
ReceivedAug 9, 1985
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K853400

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.