K-number	K150494
Device name	Proteus Digital Health Feedback Device
Applicant	Proteus Digital Health, Inc.
Product code	OZW
Device class	Class II
Decision date	Jun 27, 2015
Decision	Substantially Equivalent
Regulation	880.6305

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Source

View the full FDA submission: accessdata.fda.gov

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Proteus Digital Health Feedback Device

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