REVISED LABELING FOR SYVA BARBITURATE ASSAYS

REVISED LABELING FOR SYVA BARBITURATE ASSAYS is an FDA 510(k)-cleared medical device (K874702) manufactured by Syva Co.. 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 January 4, 1988. Regulation: 8.