QLIA T UPTAKE ASSAY

QLIA T UPTAKE ASSAY is an FDA 510(k)-cleared medical device (K883971) manufactured by Bd Becton Dickinson Vacutainer Systems Preanalytic. This device is classified under the Clinical Chemistry specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on October 24, 1988. Regulation: 8.