FDA 510(k) Applications Submitted by Vieworks Co., Ltd.

FDA 510(k) Number Submission Date Device Name Applicant
K080553 02/28/2008 DIGITAL RADIOGRAPHY SYSTEM, MODEL QXR-16 VIEWORKS CO., LTD.
K092081 07/09/2009 QXLINK VIEWORKS CO., LTD.
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.
K220239 01/28/2022 Solid State X-ray Imager(Model: FXRD-4386WB) Vieworks Co., Ltd.
K221512 05/24/2022 Vivix-S FW (Model: FXRD-2530FAW, FXRD-3643FAW, FXRD-4343FAW) Vieworks Co., Ltd.
K073056 10/30/2007 DIGITAL RADIOGRAPHY SYSTEM, MODEL: QXR-9 VIEWORKS CO., LTD.
K120020 01/03/2012 VIVIX-S VIEWORKS CO., LTD.
K132302 07/24/2013 QXLINK VIEWORKS CO., LTD.
K122865 09/18/2012 VIVIX-S WIRELESS VIEWORKS CO., LTD.
K122866 09/18/2012 VIVIX-S WITH VXVUE VIEWORKS CO., LTD.
K161113 04/20/2016 QXLink VIEWORKS CO., LTD.
K152855 09/29/2015 VIVIX-S 1012N VIEWORKS CO., LTD.


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