K-number	K142465
Device name	Aquilion ONE Vision, v7.0
Applicant	Toshibamedical Systems Corporation
Product code	JAK
Device class	Class II
Decision date	Mar 10, 2015
Decision	Substantially Equivalent
Regulation	892.1750

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View the full FDA submission: accessdata.fda.gov

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Aquilion ONE Vision, v7.0

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