K-number	K121424
Device name	EXPRESSION INFORMATION PORTAL
Applicant	Invivo Corporation
Product code	MWI
Device class	Class II
Decision date	Jun 13, 2012
Decision	Substantially Equivalent
Regulation	870.2300

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Source

View the full FDA submission: accessdata.fda.gov

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EXPRESSION INFORMATION PORTAL

Everything you need for a 510(k) submission. Nothing you don't.