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FDA 510(k) Applications Submitted by Dongguan Bohuikang Technology Co.,Ltd
FDA 510(k) Number
Submission Date
Device Name
Applicant
K213788
12/06/2021
TENS&EMS STIMULATOR (Model: KRES100D, KRES1010, KRES1020, KRES1080)
Dongguan Bohuikang Technology Co.,Ltd
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