WILKINS-CHALGREN ANAEROBE AGAR

WILKINS-CHALGREN ANAEROBE AGAR is an FDA 510(k)-cleared medical device (K811513) manufactured by Oxoid U.S.A., Inc.. This device is classified under the Microbiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on June 17, 1981. Regulation: 8.