K-number	K142567
Device name	RETeval Visual Electrodiagnostic Device
Applicant	Lkc Technologies, Inc.
Product code	GWE
Device class	Class II
Decision date	May 19, 2015
Decision	Substantially Equivalent
Regulation	882.1890

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View the full FDA submission: accessdata.fda.gov

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RETeval Visual Electrodiagnostic Device

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