UNITRON MODEL IKON AGCO/ AOD

UNITRON MODEL IKON AGCO/ AOD is an FDA 510(k)-cleared medical device (K934565) manufactured by Unitron Industries, Inc.. This device is classified under the Ear, Nose, Throat specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on November 28, 1993. Regulation: 8.