K-number	K121422
Device name	APLIO 500/400/300 DIAGNOSTIC ULTRASOUND SYSTEM
Applicant	Toshiba Medical Systems Coporation, Japan
Product code	IYO
Device class	Class II
Decision date	Aug 16, 2012
Decision	Substantially Equivalent
Regulation	892.1560

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View the full FDA submission: accessdata.fda.gov

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APLIO 500/400/300 DIAGNOSTIC ULTRASOUND SYSTEM

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