K-number	K120182
Device name	NEOMED GASTROINTESTINAL TUBE AND ACCESSORIES
Applicant	Neomed, Inc.
Product code	KNT
Device class	Class II
Decision date	Apr 19, 2012
Decision	Substantially Equivalent
Regulation	876.5980

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Source

View the full FDA submission: accessdata.fda.gov

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NEOMED GASTROINTESTINAL TUBE AND ACCESSORIES

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