K-number	K013931
Device name	OMNI OXYGEN SYSTEM, MODEL 1000
Applicant	Sequal Technologies, Inc.
Product code	CAW
Device class	Class II
Decision date	Mar 27, 2002
Decision	Substantially Equivalent
Regulation	868.5440

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View the full FDA submission: accessdata.fda.gov

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OMNI OXYGEN SYSTEM, MODEL 1000

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