IMMULITE TOXOPLASMA GONDII IGG

IMMULITE TOXOPLASMA GONDII IGG is an FDA 510(k)-cleared medical device (K950671) manufactured by Diagnostic Products Corp.. This device is classified under the Microbiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on February 22, 1996. Regulation: 8.