WIDEX MODEL LOGO 12 (L12)

WIDEX MODEL LOGO 12 (L12) is an FDA 510(k)-cleared medical device (K933640) manufactured by Widex Hearing Aid Co., Inc.. This device is classified under the Ear, Nose, Throat specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on August 22, 1993. Regulation: 8.