K-number	K161349
Device name	Everyway Incontinence Stimulation System
Applicant	Everyway Medical Instrument Co., Ltd.
Product code	KPI
Device class	Class II
Decision date	Jul 7, 2017
Decision	Substantially Equivalent
Regulation	876.5320

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View the full FDA submission: accessdata.fda.gov

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Everyway Incontinence Stimulation System

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