K-number	K172450
Device name	TENS device-HeadaTerm, eEspress
Applicant	Wat Medical Technology (Ningbo) Co., Ltd.
Product code	PCC
Device class	Class II
Decision date	Sep 13, 2018
Decision	Substantially Equivalent
Regulation	882.5891

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View the full FDA submission: accessdata.fda.gov

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TENS device-HeadaTerm, eEspress

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