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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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