K-number	K133983
Device name	INTRA. OX HANDHELD TISSUE OXIMETER
Applicant	Vioptix, Inc.
Product code	MUD
Device class	Class II
Decision date	Sep 12, 2014
Decision	Substantially Equivalent
Regulation	870.2700

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Source

View the full FDA submission: accessdata.fda.gov

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INTRA. OX HANDHELD TISSUE OXIMETER

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