SCREENERS OPIATES TEST DRUGSCREEN DIP OPIATES TEST

SCREENERS OPIATES TEST DRUGSCREEN DIP OPIATES TEST is an FDA 510(k)-cleared medical device (K000273) manufactured by Drug Detection Devices, Ltd.. 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 April 6, 2000. Regulation: 8.