FDA 510(k) Applications Submitted by Joe Xu

FDA 510(k) Number Submission Date Device Name Applicant
K220503 02/22/2022 TENS device-EmeTerm 2, Model: YF-ZTY-E2 WAT Medical Technology Inc.
K230782 03/22/2023 TENS device-HeadaTerm 2 (Model: YF-HT2) WAT Medical Technology Inc.
K172478 08/16/2017 TENS device-EmeTerm, CinvStop WAT Medical Technology (Ningbo) Co., Ltd


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