K-number	K152696
Device name	INFX-8000V, V6.20
Applicant	Toshibamedical Systems Corporation
Product code	OWB
Device class	Class II
Decision date	Jan 12, 2016
Decision	Substantially Equivalent
Regulation	892.1650

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View the full FDA submission: accessdata.fda.gov

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INFX-8000V, V6.20

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