510(k) K991120

VACUTAINER BRAND CTAD TUBE (MULTIPLE) by Becton Dickinson Vacutainer Systems — Product Code JKA

K991120 is an FDA 510(k) premarket notification submitted by Becton Dickinson Vacutainer Systems for the device "VACUTAINER BRAND CTAD TUBE (MULTIPLE)". The FDA issued a decision of Substantially Equivalent on May 19, 1999. 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 Vacutainer Systems has at least 10 other 510(k) clearances on record.