K-number	K884379
Device name	MAGLINTE ENTEROCLYSIS CATHETER
Applicant	Lafayette Pharmacal, Inc.
Product code	FGD
Device class	Class II
Decision date	Feb 28, 1989
Decision	Substantially Equivalent
Regulation	876.5980

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View the full FDA submission: accessdata.fda.gov

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MAGLINTE ENTEROCLYSIS CATHETER

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