BTE HEARING AID OTICON MODEL E39PL

BTE HEARING AID OTICON MODEL E39PL is an FDA 510(k)-cleared medical device (K874381) manufactured by Oticon Corp.. This device is classified under the Ear, Nose, Throat specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on December 22, 1987. Regulation: 8.