K-number	K895417
Device name	ARROW LARGE-BORE DUAL LUMEN HEMODIALYSIS KIT
Applicant	Arrow Intl., Inc.
Product code	LFJ
Device class	Class II
Decision date	Jan 3, 1990
Decision	Substantially Equivalent
Regulation	876.5540

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View the full FDA submission: accessdata.fda.gov

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ARROW LARGE-BORE DUAL LUMEN HEMODIALYSIS KIT

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