MILENIA (TM) DIGITOXIN

MILENIA (TM) DIGITOXIN is an FDA 510(k)-cleared medical device (K900013) 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 March 8, 1990. Regulation: 8.