K-number	K031200
Device name	MODIFICATION TO BD ULTRA-FINE III PEN NEEDLE
Applicant	Becton, Dickinson & CO
Product code	FMI
Device class	Class II
Decision date	Jun 24, 2003
Decision	Substantially Equivalent
Regulation	880.5570

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View the full FDA submission: accessdata.fda.gov

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MODIFICATION TO BD ULTRA-FINE III PEN NEEDLE

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