K-number	K133758
Device name	CENTERVUE MACULAR INTEGRITY ASSESSMENT
Applicant	Centervue S.P.A.
Product code	HLI
Device class	Class II
Decision date	Apr 23, 2014
Decision	Substantially Equivalent
Regulation	886.1570

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Source

View the full FDA submission: accessdata.fda.gov

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CENTERVUE MACULAR INTEGRITY ASSESSMENT

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