LABELING SUBMITTAL, ADX TM CANNABINOIDS-GS

LABELING SUBMITTAL, ADX TM CANNABINOIDS-GS is an FDA 510(k)-cleared medical device (K904541) manufactured by Abbott Laboratories. 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 November 19, 1990. Regulation: 8.