FDA 510(k) Applications Submitted by JORDIN KIM

FDA 510(k) Number Submission Date Device Name Applicant
K200418 02/20/2020 VIVIX-S VW Vieworks Co., Ltd.
K190611 03/11/2019 VIVIX-S 1751S Vieworks Co., Ltd.
K181003 04/16/2018 VIVIX-S 1717V Vieworks Co., Ltd.
K163703 12/29/2016 VIVIX-S 1417N VIEWORKS CO., LTD.


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