K-number	K842381
Device name	SLS 3500 LED VISUAL STIMULATOR
Applicant	Nihon Kohden America, Inc.
Product code	GWE
Device class	Class II
Decision date	Nov 9, 1984
Decision	Substantially Equivalent
Regulation	882.1890

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View the full FDA submission: accessdata.fda.gov

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SLS 3500 LED VISUAL STIMULATOR

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