ADVANCE TM T-3 UPTAKE ASSAY

ADVANCE TM T-3 UPTAKE ASSAY is an FDA 510(k)-cleared medical device (K822592) manufactured by Syva Co.. 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 7, 1982. Regulation: 8.