K-number	K810499
Device name	PERCUTANEOUS GASTROINTESTINAL TUBE
Applicant	Health Development Corp.
Product code	KNT
Device class	Class II
Decision date	Mar 4, 1981
Decision	Substantially Equivalent
Regulation	876.5980

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View the full FDA submission: accessdata.fda.gov

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PERCUTANEOUS GASTROINTESTINAL TUBE

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