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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