K-number	K841497
Device name	NEUROPACK 8 MEE 4108
Applicant	Nihon Kohden America, Inc.
Product code	GWK
Device class	Class II
Decision date	Jun 7, 1984
Decision	Substantially Equivalent
Regulation	882.1845

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View the full FDA submission: accessdata.fda.gov

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NEUROPACK 8 MEE 4108

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