K-number	K120785
Device name	OMNI 3 OXYGEN SYSTEM
Applicant	Caire, Inc.
Product code	CAW
Device class	Class II
Decision date	Oct 25, 2012
Decision	Substantially Equivalent
Regulation	868.5440

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View the full FDA submission: accessdata.fda.gov

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OMNI 3 OXYGEN SYSTEM

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