
Biosite Incorporated
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TRIAGE TOX DRUG SCREEN CALIBRATION VERIFICATION CONTROLS, CATALOG #94002 is an FDA 510(k)-cleared medical device (K013002) manufactured by Biosite Incorporated. This device is classified under the Clinical Toxicology specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on October 2, 2001. Regulation: 8.