K-number	K100095
Device name	CENTRAL VISION ANALYZER MODEL 1000
Applicant	Vimetrics,Llc.
Product code	HOX
Device class	Class I
Decision date	May 10, 2010
Decision	Substantially Equivalent
Regulation	886.1150

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View the full FDA submission: accessdata.fda.gov

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CENTRAL VISION ANALYZER MODEL 1000

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