WIDEX MODEL LOGO 32 (L32)

WIDEX MODEL LOGO 32 (L32) is an FDA 510(k)-cleared medical device (K952229) 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 June 18, 1995. Regulation: 8.