FDA 510(k) Applications Submitted by Belinda Dueholm

FDA 510(k) Number Submission Date Device Name Applicant
K150961 04/10/2015 EmbryoSlide Culture Dish VITROLIFE A/S
K182798 10/02/2018 KIDScore D3 Vitrolife A/S
K173264 10/11/2017 EmbryoScope+ Vitrolife A/S
K213869 12/13/2021 EmbryoSlide+ ic8 dish Vitrolife A/S


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