
Bio-Rad
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LIQUICHEK URINE TOXICOLOGY CONTROL - LEVEL S1, S2, S3 is an FDA 510(k)-cleared medical device (K971691) 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 May 29, 1997. Regulation: 8.