K-number	K092039
Device name	IDENTEVENT, VERSION 1.0G
Applicant	Optima Neuroscience, Inc.
Product code	OMB
Device class	Class II
Decision date	Oct 16, 2009
Decision	Substantially Equivalent
Regulation	882.1400

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View the full FDA submission: accessdata.fda.gov

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IDENTEVENT, VERSION 1.0G

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