LEGIONELLA INDIRECT FLUOR. ANTIBODY

LEGIONELLA INDIRECT FLUOR. ANTIBODY is an FDA 510(k)-cleared medical device (K812007) manufactured by Centers for Disease Control and Prevention. This device is classified under the Microbiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on September 7, 1981. Regulation: 8.