K-number	K131789
Device name	CEREBRALOGIK- AEEG
Applicant	Mennen Medical , Ltd.
Product code	OMA
Device class	Class II
Decision date	Dec 27, 2013
Decision	Substantially Equivalent
Regulation	882.1400

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View the full FDA submission: accessdata.fda.gov

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CEREBRALOGIK- AEEG

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