K-number	K172863
Device name	Infinix-i, INFX-8000V, V7.0
Applicant	Toshibamedical Systems Corporation
Product code	OWB
Device class	Class II
Decision date	Dec 14, 2017
Decision	Substantially Equivalent
Regulation	892.1650

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View the full FDA submission: accessdata.fda.gov

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Infinix-i, INFX-8000V, V7.0

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