
Drial Consultants, Inc.
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QUIKPAC II ONE STEP OPIATE TEST is an FDA 510(k)-cleared medical device (K972405) manufactured by Drial Consultants, 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 August 7, 1997. Regulation: 8.