K-number	K163094
Device name	TinniLogic Mobile Tinnitus Management Device
Applicant	Jiangsu Betterlife Medical Co., Ltd.
Product code	KLW
Device class	Class II
Decision date	May 17, 2017
Decision	Substantially Equivalent
Regulation	874.3400

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Source

View the full FDA submission: accessdata.fda.gov

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TinniLogic Mobile Tinnitus Management Device

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