CYTOMEGALOVIRUS IGG EIA KIT

CYTOMEGALOVIRUS IGG EIA KIT is an FDA 510(k)-cleared medical device (K880433) manufactured by De Ferris Laboratories, 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 March 26, 1989. Regulation: 8.