WIDEX MODEL SENSO DIGITAL (C8)

WIDEX MODEL SENSO DIGITAL (C8) is an FDA 510(k)-cleared medical device (K955878) 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 February 11, 1996. Regulation: 8.