DUPONT ACA(R) URINE DRUGE OS ABUSE CONTROL

DUPONT ACA(R) URINE DRUGE OS ABUSE CONTROL is an FDA 510(k)-cleared medical device (K952412) manufactured by Dupont Medical Products. This device is classified under the Clinical Toxicology specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on June 22, 1995. Regulation: 8.