FIRST CHECK HOME DRUG TEST PANEL 3

FIRST CHECK HOME DRUG TEST PANEL 3 is an FDA 510(k)-cleared medical device (K994138) manufactured by Worldwide Medical 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 22, 2000. Regulation: 8.