WIDEX SENSO DIGITAL (PX)

WIDEX SENSO DIGITAL (PX) is an FDA 510(k)-cleared medical device (K954526) 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 October 17, 1995. Regulation: 8.