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Phamatech, Inc.
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QUICKSCREEN OXYCODONE TEST, MODELS 9120, 9120T, 9120X AND 9121 is an FDA 510(k)-cleared medical device (K043051) manufactured by Phamatech, 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 February 6, 2005. Regulation: 8.