K-number	K213116
Device name	Everyway Incontinence Stimulation System
Applicant	Everyway Medical Instruments Co.,Ltd
Product code	KPI
Device class	Class II
Decision date	Dec 3, 2021
Decision	Substantially Equivalent
Regulation	876.5320

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Source

View the full FDA submission: accessdata.fda.gov

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Everyway Incontinence Stimulation System

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