K-number	K173931
Device name	MindMotion(TM) GO
Applicant	Mindmaze SA
Product code	LXJ
Device class	Class II
Decision date	May 17, 2018
Decision	Substantially Equivalent
Regulation	890.5360

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Source

View the full FDA submission: accessdata.fda.gov

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MindMotion(TM) GO

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