FDA 510(k) Applications Submitted by BUHLMANN Laboratories AG

FDA 510(k) Number Submission Date Device Name Applicant
K181012 04/17/2018 BUHLMANN fCAL ELISA BUHLMANN Laboratories AG
K190784 03/27/2019 BUHLMANN fCAL turbo BUHLMANN Laboratories AG
K191718 06/26/2019 Buhlmann fCAL turbo and CALEX Cap BUHLMANN Laboratories AG


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