QUICKSCREEN PRO MULTI DRUG SCREEN, MODEL 9177 & 9178

QUICKSCREEN PRO MULTI DRUG SCREEN, MODEL 9177 & 9178 is an FDA 510(k)-cleared medical device (K993165) manufactured by Phamatech. 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 October 19, 1999. Regulation: 8.