NEIA-FERRITIN ENZYMEIMMUNOASSAY

NEIA-FERRITIN ENZYMEIMMUNOASSAY is an FDA 510(k)-cleared medical device (K780490) manufactured by New England Immunology Assoc.. This device is classified under the Immunology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on April 9, 1978. Regulation: 8.