K-number	K053410
Device name	GIENTRIPORT WITH UNIVERSAL SINGLE LUMEN ADAPTOR
Applicant	Kendall
Product code	FEG
Device class	Class II
Decision date	Jan 6, 2006
Decision	Substantially Equivalent
Regulation	876.5980

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Source

View the full FDA submission: accessdata.fda.gov

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GIENTRIPORT WITH UNIVERSAL SINGLE LUMEN ADAPTOR

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