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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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