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FDA 510(k) Applications Submitted by Ke Xi
FDA 510(k) Number
Submission Date
Device Name
Applicant
K160932
04/04/2016
8ch Foot Ankle Coil
Shenzhen RF Tech Co., Ltd.
K160935
04/04/2016
8ch Foot Ankle Coil
Shenzhen RF Tech Co., Ltd.
K151653
06/18/2015
8ch Foot Ankle Coil
SHENZHEN RFTECH CO., LTD.
K172222
07/24/2017
8ch Flex Suite
Shenzhen RF Tech Co., Ltd.
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