K-number	K102388
Device name	VIVID I DIAGNOSTIC ULTRASOUND SYSTEM
Applicant	Ge Medical System Israel , Ltd.
Product code	IYN
Device class	Class II
Decision date	Nov 4, 2010
Decision	Substantially Equivalent
Regulation	892.1550

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View the full FDA submission: accessdata.fda.gov

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VIVID I DIAGNOSTIC ULTRASOUND SYSTEM

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