K-number	K072602
Device name	VACUETTE PREMIUM SAFETY NEEDLE SYSTEM
Applicant	Medpro Safety Products, Inc.
Product code	FMI
Device class	Class II
Decision date	Jun 18, 2008
Decision	Substantially Equivalent
Regulation	880.5570

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Source

View the full FDA submission: accessdata.fda.gov

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VACUETTE PREMIUM SAFETY NEEDLE SYSTEM

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