K-number	K132314
Device name	MEDLINE ANTI-REFLUX VALVE
Applicant	Medline Industries, Inc.
Product code	FEG
Device class	Class II
Decision date	Sep 18, 2013
Decision	Substantially Equivalent
Regulation	876.5980

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Source

View the full FDA submission: accessdata.fda.gov

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MEDLINE ANTI-REFLUX VALVE

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