ENZYGNOST ANTIHERPES SIMPLEX VIRUS

ENZYGNOST ANTIHERPES SIMPLEX VIRUS is an FDA 510(k)-cleared medical device (K841245) manufactured by Behring 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 November 4, 1985. Regulation: 8.