K-number	K142794
Device name	Everyway Facial MENS
Applicant	Everyway Medical Instruments Co.,Ltd
Product code	NFO
Device class	Class II
Decision date	Jun 2, 2015
Decision	Substantially Equivalent
Regulation	882.5890

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Source

View the full FDA submission: accessdata.fda.gov

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Everyway Facial MENS

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