K-number	K100456
Device name	CVUE ADVANCED DEFINITIVE
Applicant	Unilens Corp., USA
Product code	LPL
Device class	Class II
Decision date	Oct 28, 2010
Decision	Substantially Equivalent
Regulation	886.5925

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Source

View the full FDA submission: accessdata.fda.gov

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CVUE ADVANCED DEFINITIVE

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