TETRAHYDROCANNALBINOL DIRECT BLOOD KIT

TETRAHYDROCANNALBINOL DIRECT BLOOD KIT is an FDA 510(k)-cleared medical device (K791649) manufactured by Immunalysis Corporation. 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 October 10, 1979. Regulation: 8.