ClearanceBrief
510(k) K862540 ยท DWD Suction Control, Intracardiac, Cardiopulmonary Bypass

LEFT VENTRICULAR VENT VALVE MODEL NO. GLV

ApplicantGish Biomedical, Inc., Santa Ana CA, US
DecisionSubstantially Equivalent, Aug 29, 1986
ReceivedJul 2, 1986
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K862540

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.