BRAHMS DIAGNOSTICA DYNOTEST ANTI-TG

BRAHMS DIAGNOSTICA DYNOTEST ANTI-TG is an FDA 510(k)-cleared medical device (K992790) manufactured by Brahms Diagnostica, LLC. This device is classified under the Immunology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on November 11, 1999. Regulation: 8.