K-number	K162991
Device name	YELLOW 560 Fluorescence Module
Applicant	Carl Zeiss Meditec, AG
Product code	IZI
Device class	Class II
Decision date	Jul 24, 2017
Decision	Substantially Equivalent — Same Device
Regulation	892.1600

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Source

View the full FDA submission: accessdata.fda.gov

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YELLOW 560 Fluorescence Module

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