K-number	DEN120015
Device name	EEVA 2.0
Applicant	Auxogyn, Inc.
Product code	PBH
Device class	Class II
Decision date	Jun 6, 2014
Decision	Not Substantially Equivalent
Regulation	884.6195

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Source

View the full FDA submission: accessdata.fda.gov

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EEVA 2.0

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