LIQUICHEK URINE TOXICOLOGY CONTROL, (LEVELS S1S AND S2S)

LIQUICHEK URINE TOXICOLOGY CONTROL, (LEVELS S1S AND S2S) is an FDA 510(k)-cleared medical device (K042865) 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 November 23, 2004. Regulation: 8.