K-number	K130238
Device name	NIHON KOHDEN AE-918P NEURO UNIT
Applicant	Nihon Kohden Corp.
Product code	OMA
Device class	Class II
Decision date	Mar 4, 2015
Decision	Substantially Equivalent
Regulation	882.1400

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View the full FDA submission: accessdata.fda.gov

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NIHON KOHDEN AE-918P NEURO UNIT

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