ABUSCREEN FP FOR AMPHETAMINE

ABUSCREEN FP FOR AMPHETAMINE is an FDA 510(k)-cleared medical device (K890886) manufactured by Roche Diagnostic Systems, Inc.. This device is classified under the Clinical Toxicology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on March 9, 1989. Regulation: 8.