
Medtox Diagnostics, Inc.
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VERDICT -II TCA, VERDICT-II MTD is an FDA 510(k)-cleared medical device (K011545) manufactured by Medtox Diagnostics, 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 June 7, 2001. Regulation: 8.