K-number	K103833
Device name	NEOPIP PATIENT CIRCUIT WITH PEEP
Applicant	Neoforce Group, Inc.
Product code	BYE
Device class	Class II
Decision date	Apr 20, 2011
Decision	Substantially Equivalent
Regulation	868.5965

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Source

View the full FDA submission: accessdata.fda.gov

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NEOPIP PATIENT CIRCUIT WITH PEEP

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