K-number	K971354
Device name	KNOTT NG TUBE
Applicant	Michael M. Knott, M.D.
Product code	FEG
Device class	Class II
Decision date	Nov 19, 1997
Decision	Substantially Equivalent
Regulation	876.5980

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View the full FDA submission: accessdata.fda.gov

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KNOTT NG TUBE

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