K-number	K163472
Device name	Intra.Ox Handheld Tissue Oximeter
Applicant	Vioptix, Inc.
Product code	MUD
Device class	Class II
Decision date	Nov 16, 2017
Decision	Substantially Equivalent
Regulation	870.2700

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View the full FDA submission: accessdata.fda.gov

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Intra.Ox Handheld Tissue Oximeter

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