K-number	K100209
Device name	BD ECLIPSE NEEDLE WITH SMARTSLIP TECHNOLOGY
Applicant	Becton, Dickinson & CO
Product code	FMI
Device class	Class II
Decision date	Feb 19, 2010
Decision	Substantially Equivalent
Regulation	880.5570

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View the full FDA submission: accessdata.fda.gov

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BD ECLIPSE NEEDLE WITH SMARTSLIP TECHNOLOGY

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