
Dade Behring, Inc.
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URINE AMPHETAMINE/METHAMPHETAMINE (AMPH) SCREEN FLEX REAGENT, CATALOG NO. DF 90A is an FDA 510(k)-cleared medical device (K000460) manufactured by Dade Behring, 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 April 13, 2000. Regulation: 8.