
Utak Laboratories, Inc.
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AMOXAPINE 8-HYDRO-XYAMOXAPINE is an FDA 510(k)-cleared medical device (K831734) manufactured by Utak Laboratories, Inc.. This device is classified under the Clinical Toxicology specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on July 25, 1983. Regulation: 8.