FDA 510(k) Applications Submitted by Gary Wang

FDA 510(k) Number Submission Date Device Name Applicant
K200836 03/31/2020 8ch Flex Suite Shenzhen RF Tech Co., Ltd.
K223203 10/14/2022 1.5T 24E Posterior Array Shenzhen RF Tech Co., Ltd.
K223225 10/18/2022 8ch T/R Knee Coil Shenzhen RF Tech Co., Ltd.
K223239 10/20/2022 8ch Wrist Coil Shenzhen RF Tech Co., Ltd.


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