GILFORD UNIQUAL ABNORMAL CONTROL SERUM/ASSAYED

GILFORD UNIQUAL ABNORMAL CONTROL SERUM/ASSAYED is an FDA 510(k)-cleared medical device (K860999) manufactured by Ciba Corning Diagnostics Corp.. This device is classified under the Clinical Chemistry specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on July 1, 1986. Regulation: 8.