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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