K-number	K854663
Device name	NEUROFAX 7310 SERIES (EEG)
Applicant	Nihon Kohden America, Inc.
Product code	GWQ
Device class	Class II
Decision date	Aug 20, 1986
Decision	Substantially Equivalent
Regulation	882.1400

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View the full FDA submission: accessdata.fda.gov

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NEUROFAX 7310 SERIES (EEG)

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