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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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