LAS-R CERULOPLASMIN TEST

LAS-R CERULOPLASMIN TEST is an FDA 510(k)-cleared medical device (K771795) manufactured by Hyland Therapeutic Div., Travenol Laboratories. This device is classified under the Immunology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on November 13, 1977. Regulation: 8.