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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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