K-number	K094064
Device name	ILUMA VISION MODEL VERSION 2.2
Applicant	3M Imtec
Product code	LLZ
Device class	Class II
Decision date	Apr 30, 2010
Decision	Substantially Equivalent
Regulation	892.2050

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View the full FDA submission: accessdata.fda.gov

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ILUMA VISION MODEL VERSION 2.2

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