LIQUICHEK(R) SERUM ALCOHOL CONTROL; LEVELS 1,2 & 3

LIQUICHEK(R) SERUM ALCOHOL CONTROL; LEVELS 1,2 & 3 is an FDA 510(k)-cleared medical device (K892004) manufactured by Bio-Rad. This device is classified under the Clinical Toxicology specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on April 20, 1989. Regulation: 8.