MUELLER HINTON AGAR, POURED INTO A PLATE

MUELLER HINTON AGAR, POURED INTO A PLATE is an FDA 510(k)-cleared medical device (K811472) manufactured by Biomedia, 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.