K-number	K162110
Device name	CORGRIP NG/NI Tube Retention System
Applicant	Corpak Medsystems, Inc. A Division of Haylard Health
Product code	KNT
Device class	Class II
Decision date	Sep 15, 2016
Decision	Unknown
Regulation	876.5980

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Source

View the full FDA submission: accessdata.fda.gov

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CORGRIP NG/NI Tube Retention System

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