FDA 510(k) Applications Submitted by Vitromed GmbH

FDA 510(k) Number Submission Date Device Name Applicant
K192146 08/08/2019 V-DENUPET Vitromed GmbH
K193285 11/27/2019 V-ONESTEP Vitromed GmbH
K222606 08/29/2022 V-HYADASE VITROMED GmbH
K223117 10/03/2022 V-SPERM WASH Vitromed GmbH


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