K-number	K080235
Device name	SAFETY INFUSION SET
Applicant	Greiner Bio-One Vacuette North America
Product code	FMI
Device class	Class II
Decision date	Apr 24, 2008
Decision	Substantially Equivalent
Regulation	880.5570

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Source

View the full FDA submission: accessdata.fda.gov

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SAFETY INFUSION SET

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