BENZODIAZEPINE ENZYME IMMUNOASSAY KIT

BENZODIAZEPINE ENZYME IMMUNOASSAY KIT is an FDA 510(k)-cleared medical device (K863877) manufactured by General Diagnostics. 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 11, 1987. Regulation: 8.