K-number	K112680
Device name	EVIS EXERA III VIDEO SYSTEM
Applicant	Olympus Medical Systems Corporation
Product code	FDF
Device class	Class II
Decision date	Feb 16, 2012
Decision	Substantially Equivalent
Regulation	876.1500

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Source

View the full FDA submission: accessdata.fda.gov

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EVIS EXERA III VIDEO SYSTEM

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