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FDA 510(k) Applications Submitted by Anja Bengtzelius
FDA 510(k) Number
Submission Date
Device Name
Applicant
K172050
07/06/2017
Follicle Aspiration Set, Reduced Single Lumen
Vitrolife Sweden AB
K161970
07/18/2016
Follicle Aspiration Set
VITROLIFE SWEDEN AB
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