K-number	K841612
Device name	NEUROPACK II 5100
Applicant	Nihon Kohden America, Inc.
Product code	GWL
Device class	Class II
Decision date	Jun 7, 1984
Decision	Substantially Equivalent
Regulation	882.1835

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View the full FDA submission: accessdata.fda.gov

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NEUROPACK II 5100

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