VISTA ANTIGEN BRUCELLA ABORTUS

VISTA ANTIGEN BRUCELLA ABORTUS is an FDA 510(k)-cleared medical device (K972394) manufactured by Lee Laboratories, 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 August 24, 1997. Regulation: 8.