FDA 510(k) Applications Submitted by DEXCOWIN CO., LTD

FDA 510(k) Number Submission Date Device Name Applicant
K133007 09/25/2013 DX3000-L DEXCOWIN CO., LTD
K134055 12/31/2013 ADX4000W DEXCOWIN CO., LTD
K083532 11/28/2008 ADX4000-L, DX3000-L DEXCOWIN CO., LTD
K143494 12/09/2014 ADX6000 Portable X-Ray System; iRayA6 DEXCOWIN CO., LTD


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