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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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