FDA 510(k) Applications Submitted by MAPQUET CARDIOPULMONARY AG

FDA 510(k) Number Submission Date Device Name Applicant
K082412 08/21/2008 VENOUS BUBBLE TRAP, MODEL VBT 160; VENOUS BUBBLE TRAP WITH BIOLINE COATING, MODEL BE-VBT 160, BEQ-VBT 160 MAPQUET CARDIOPULMONARY AG


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