K-number	K120870
Device name	GREENLIGHT MOXY FIBER OPTIC
Applicant	American Medical Systems
Product code	GEX
Device class	Class II
Decision date	Jun 15, 2012
Decision	Substantially Equivalent
Regulation	878.4810

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Source

View the full FDA submission: accessdata.fda.gov

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GREENLIGHT MOXY FIBER OPTIC

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