HERPES VIRUS HOMINIS ANTIBODY TEST SYS.

HERPES VIRUS HOMINIS ANTIBODY TEST SYS. is an FDA 510(k)-cleared medical device (K812085) manufactured by Zeus Scientific, 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 August 31, 1981. Regulation: 8.