K-number	K880850
Device name	KEITH NASOGASTRIC SUMP TUBE W/ANTI-REFLUX VALVE
Applicant	Kmb Medical Products Co.
Product code	FEG
Device class	Class II
Decision date	May 26, 1988
Decision	Substantially Equivalent
Regulation	876.5980

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View the full FDA submission: accessdata.fda.gov

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KEITH NASOGASTRIC SUMP TUBE W/ANTI-REFLUX VALVE

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