FIRST CHECK HOME DRUG TEST PANEL 4

FIRST CHECK HOME DRUG TEST PANEL 4 is an FDA 510(k)-cleared medical device (K993852) 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 November 28, 2000. Regulation: 8.