LAS-R HUMAN PLASMINOGEN TEST

LAS-R HUMAN PLASMINOGEN TEST is an FDA 510(k)-cleared medical device (K772085) manufactured by Hyland Therapeutic Div., Travenol Laboratories. This device is classified under the Immunology specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on January 23, 1978. Regulation: 8.