510(k) K172670

BD Single Use, Hypodermic Syringe by Becton, Dickinson And Company — Product Code FMF

K172670 is an FDA 510(k) premarket notification submitted by Becton, Dickinson And Company for the device "BD Single Use, Hypodermic Syringe". The FDA issued a decision of Substantially Equivalent on Oct 23, 2018. The device falls under product code FMF (Syringe, Piston), a Class II device regulated under 21 CFR 880.5860. Becton, Dickinson And Company has 329 other 510(k) clearances on record.