K-number	K170667
Device name	QEVO System with KINEVO 900
Applicant	Carl Zeiss Meditec, AG
Product code	GWG
Device class	Class II
Decision date	Aug 18, 2017
Decision	Substantially Equivalent
Regulation	882.1480

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Source

View the full FDA submission: accessdata.fda.gov

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QEVO System with KINEVO 900

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