LAS-R HUMAN IGD TEST

LAS-R HUMAN IGD TEST is an FDA 510(k)-cleared medical device (K772327) 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 February 27, 1978. Regulation: 8.