(125 I) DIGITOXIN RIA KIT

(125 I) DIGITOXIN RIA KIT is an FDA 510(k)-cleared medical device (K780766) manufactured by Diagnostic Products 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 July 26, 1978. Regulation: 8.