510(k) K231237

BD Vacutainer® Fluoride Blood Collection Tubes by Becton, Dickinson and Company — Product Code JKA

K231237 is an FDA 510(k) premarket notification submitted by Becton, Dickinson and Company for the device "BD Vacutainer® Fluoride Blood Collection Tubes". The FDA issued a decision of Substantially Equivalent on January 19, 2024. The device falls under product code JKA (Tubes, Vials, Systems, Serum Separators, Blood Collection), a Class II device regulated under 21 CFR 862.1675. Becton, Dickinson and Company has at least 10 other 510(k) clearances on record.