K-number	K112546
Device name	O_TWO CPAP SYSTEM
Applicant	O-Two Medical Technologies, Inc.
Product code	BYE
Device class	Class II
Decision date	Dec 27, 2011
Decision	Substantially Equivalent
Regulation	868.5965

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View the full FDA submission: accessdata.fda.gov

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O_TWO CPAP SYSTEM

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