SEARS BEHIND-THE-EAR HEARING AID

SEARS BEHIND-THE-EAR HEARING AID is an FDA 510(k)-cleared medical device (K800113) manufactured by Int'L Hearing Aids, 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 10, 1980. Regulation: 8.