125 I DIGOXIN RIA KIT

125 I DIGOXIN RIA KIT is an FDA 510(k)-cleared medical device (K771525) 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 October 13, 1977. Regulation: 8.