SAS SALMONELLA O GROUP Q FACTOR 39 ANTISERUM

SAS SALMONELLA O GROUP Q FACTOR 39 ANTISERUM is an FDA 510(k)-cleared medical device (K960462) 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 March 5, 1996. Regulation: 8.