LISTERIA SELECTIVE MEDIUM (OXFORD FORMULATION)

LISTERIA SELECTIVE MEDIUM (OXFORD FORMULATION) is an FDA 510(k)-cleared medical device (K884208) manufactured by Oxoid U.S.A., Inc.. This device is classified under the Microbiology specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on October 24, 1988. Regulation: 8.