K-number	K123500
Device name	AQUILION LB TRITON V4.91
Applicant	Toshibamedical Systems Corporation
Product code	JAK
Device class	Class II
Decision date	May 2, 2013
Decision	Substantially Equivalent
Regulation	892.1750

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View the full FDA submission: accessdata.fda.gov

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AQUILION LB TRITON V4.91

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