LIQUICHEK CK-MB CONTROL LEVELS 1,2, AND3

LIQUICHEK CK-MB CONTROL LEVELS 1,2, AND3 is an FDA 510(k)-cleared medical device (K925151) manufactured by Bio-Rad. This device is classified under the Clinical Chemistry specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on December 16, 1992. Regulation: 8.