
Travenol Laboratories, S.A.
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Q-PAK URINE TOXICOLOGY CONTROL UNASSAYED is an FDA 510(k)-cleared medical device (K821950) manufactured by Travenol Laboratories, S.A.. This device is classified under the Clinical Toxicology specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on July 19, 1982. Regulation: 8.