
Iagnon Corp.
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DIAGNON FERRITIN 125 I RIA KIT is an FDA 510(k)-cleared medical device (K830580) manufactured by Iagnon Corp.. This device is classified under the Immunology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on May 4, 1983. Regulation: 8.