VARICELLA-ZOSTER VIRUS ANTIBODY TEST KIT-LATEX AGG

VARICELLA-ZOSTER VIRUS ANTIBODY TEST KIT-LATEX AGG is an FDA 510(k)-cleared medical device (K903882) manufactured by Viral Antigens, 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 December 3, 1990. Regulation: 8.