LIQUID CARDIAC MARKER 1,2,3 ASSAYED

LIQUID CARDIAC MARKER 1,2,3 ASSAYED is an FDA 510(k)-cleared medical device (K960246) 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 April 22, 1996. Regulation: 8.