FIAX TEST KIT FOR HERPES SIMPLEX VIRUS

FIAX TEST KIT FOR HERPES SIMPLEX VIRUS is an FDA 510(k)-cleared medical device (K792559) manufactured by Intl. Diagnostic Technology. This device is classified under the Microbiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on March 2, 1980. Regulation: 8.