
U.S. Drug Testing, Inc.
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AMPHETAMINE TEST SYSTEM is an FDA 510(k)-cleared medical device (K934693) manufactured by U.S. Drug Testing, 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 November 21, 1993. Regulation: 8.