K-number	K151870
Device name	BD U-500 INSULIN SYRINGE
Applicant	Becton, Dickinson and Company
Product code	FMF
Device class	Class II
Decision date	Jul 8, 2016
Decision	Substantially Equivalent
Regulation	880.5860

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View the full FDA submission: accessdata.fda.gov

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BD U-500 INSULIN SYRINGE

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