K-number	K950597
Device name	CORE-RESISTANT HUBER INFUSION SET WITH Y-SITE
Applicant	Distronic Sterile Products, Inc.
Product code	FPA
Device class	Class II
Decision date	Jul 26, 1995
Decision	Substantially Equivalent
Regulation	880.5440

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CORE-RESISTANT HUBER INFUSION SET WITH Y-SITE

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