ENZYGNOST ANTI-VZV IGG TEST

ENZYGNOST ANTI-VZV IGG TEST is an FDA 510(k)-cleared medical device (K863317) 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 April 21, 1987. Regulation: 8.