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Recognized a 510(k)/PMA number — showing its clearance record and devices.

Clearance record K181003

VIVIX-S 1717V · Vieworks Co., Ltd. · decided 2018-05-15 (SESE)

FDA 510(k) database ↗Summary PDF ↗

Devices

BrandModelCompanyProduct codesPrimary DI
VIVIX-S 1717VFXRD-1717VBVIEWORKS CO., LTD.MQB08809394330258
VIVIX-S 1717VFXRD-1717VAVIEWORKS CO., LTD.MQB08809394330241