K-number	K070606
Device name	VISIO+CD VIEWER# KPSCDVE01
Applicant	Keosys Sas
Product code	LLZ
Device class	Class II
Decision date	Apr 24, 2007
Decision	Substantially Equivalent
Regulation	892.2050

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Source

View the full FDA submission: accessdata.fda.gov

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VISIO+CD VIEWER# KPSCDVE01

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