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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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