K-number	K072079
Device name	IGUIDE SYSTEM
Applicant	Medical Intelligence Medizintechnik-GmbH-An Elekta
Product code	IYE
Device class	Class II
Decision date	Aug 14, 2007
Decision	Substantially Equivalent
Regulation	892.5050

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Source

View the full FDA submission: accessdata.fda.gov

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IGUIDE SYSTEM

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