
Diagnostic Products Corp.
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DOUBLE ANTIBODY CANNABINOIDS KTHD1 AND KTHD5 is an FDA 510(k)-cleared medical device (K871695) manufactured by Diagnostic Products Corp.. 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 4, 1987. Regulation: 8.