RAPID DRUG SCREEN' 8 PANEL

RAPID DRUG SCREEN' 8 PANEL is an FDA 510(k)-cleared medical device (K980872) manufactured by American Bio Medica 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 March 19, 1998. Regulation: 8.