K-number	K123399
Device name	MYOVISION 3.0 WIREFREE SYSTEM
Applicant	Precision Biometrics, Inc.
Product code	IKN
Device class	Class II
Decision date	Aug 1, 2013
Decision	Substantially Equivalent
Regulation	890.1375

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Source

View the full FDA submission: accessdata.fda.gov

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MYOVISION 3.0 WIREFREE SYSTEM

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