SAS BRUCELLA SUIS ANTISERUM

SAS BRUCELLA SUIS ANTISERUM is an FDA 510(k)-cleared medical device (K952144) manufactured by Sa Scientific, 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 July 20, 1995. Regulation: 8.