
Microgenics Corp.
Free shipping on orders over $99 · 30-day returns
CEDIA DAU BARBITURATE ASSAY is an FDA 510(k)-cleared medical device (K936030) manufactured by Microgenics 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 March 21, 1994. Regulation: 8.