K-number	K091518
Device name	CUBESCAN BIOCON-500 DIAGNOSTIC ULTRASOUND SYSTEM
Applicant	Mcube Technology Co., Ltd.
Product code	IYO
Device class	Class II
Decision date	Jun 18, 2009
Decision	Substantially Equivalent
Regulation	892.1560

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View the full FDA submission: accessdata.fda.gov

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CUBESCAN BIOCON-500 DIAGNOSTIC ULTRASOUND SYSTEM

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