MUELLER HINTON AGAR WITH 2% NACI

MUELLER HINTON AGAR WITH 2% NACI is an FDA 510(k)-cleared medical device (K960313) manufactured by Remel, L.P.. This device is classified under the Microbiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on March 24, 1996. Regulation: 8.