ADPIFA TEST FOR ANTIBODIES TO TOXOPLASMA GONDII

ADPIFA TEST FOR ANTIBODIES TO TOXOPLASMA GONDII is an FDA 510(k)-cleared medical device (K844287) manufactured by Apple Diagnostic Products. This device is classified under the Microbiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on January 6, 1985. Regulation: 8.