K-number	K090866
Device name	NEUROCALM MODEL 1 AND 2
Applicant	Neuromed Devices, Inc.
Product code	GZJ
Device class	Class II
Decision date	Oct 21, 2009
Decision	Substantially Equivalent
Regulation	882.5890

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Source

View the full FDA submission: accessdata.fda.gov

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NEUROCALM MODEL 1 AND 2

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