K-number	K130648
Device name	FORUM GLAUCOMA WORKPLACE
Applicant	Carl Zeiss Meditec, AG
Product code	NFJ
Device class	Class II
Decision date	Jul 23, 2013
Decision	Substantially Equivalent
Regulation	892.2050

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Source

View the full FDA submission: accessdata.fda.gov

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FORUM GLAUCOMA WORKPLACE

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