MODIFICA-OF EMIT AED PRIMIDONE ASSAY

MODIFICA-OF EMIT AED PRIMIDONE ASSAY is an FDA 510(k)-cleared medical device (K832798) 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 October 13, 1983. Regulation: 8.