EIA KIT FOR THE DETECTION OF GBM ANTIBODIES

EIA KIT FOR THE DETECTION OF GBM ANTIBODIES is an FDA 510(k)-cleared medical device (K953495) manufactured by Scimedx Corp.. This device is classified under the Immunology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on April 9, 1996. Regulation: 8.