TOXOPLASMA GONDII IGG

TOXOPLASMA GONDII IGG is an FDA 510(k)-cleared medical device (K902792) manufactured by Pharmacia Diagnostics, 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 July 23, 1990. Regulation: 8.