AST/SGOT LIQUID REAGENT - KINETIC METHOD

AST/SGOT LIQUID REAGENT - KINETIC METHOD is an FDA 510(k)-cleared medical device (K981650) manufactured by Teco Diagnostics. 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 June 28, 1998. Regulation: 8.