K-number	K081940
Device name	AVALON ELITE VASCULAR ACCESS KIT
Applicant	Avalon Laboratories, LLC
Product code	DRE
Device class	Class II
Decision date	Nov 18, 2008
Decision	Substantially Equivalent
Regulation	870.1310

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View the full FDA submission: accessdata.fda.gov

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AVALON ELITE VASCULAR ACCESS KIT

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