
Scimedx Corp.
Free shipping on orders over $99 · 30-day returns
PHASE II GBM IGG ANTIBODY EIA TEST is an FDA 510(k)-cleared medical device (K011348) 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 June 24, 2001. Regulation: 8.