K-number	K802300
Device name	VIVONEX JEJUNOSTOMY KIT
Applicant	Norwich Eaton Pharmaceuticals, Inc.
Product code	KNT
Device class	Class II
Decision date	Oct 23, 1980
Decision	Substantially Equivalent
Regulation	876.5980

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View the full FDA submission: accessdata.fda.gov

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VIVONEX JEJUNOSTOMY KIT

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