
Dyna-Tek Industries
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DE-TOX CONTROL 1 AND DE-TOX CONTROL 19 is an FDA 510(k)-cleared medical device (K964771) manufactured by Dyna-Tek Industries. This device is classified under the Clinical Toxicology specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on February 3, 1997. Regulation: 8.