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Ucp Biosciences, Inc.
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UCP RAPID DRUG SCREENING TRICYCLIC ANTIDEPRESSANT, PROPOXYPHENE TESTS is an FDA 510(k)-cleared medical device (K061457) manufactured by Ucp Biosciences, 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 20, 2006. Regulation: 8.