RESOUND HES, DIGITALLY PROGR., ITE HEARING AID

RESOUND HES, DIGITALLY PROGR., ITE HEARING AID is an FDA 510(k)-cleared medical device (K884871) manufactured by Resound Corp.. This device is classified under the Ear, Nose, Throat specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on February 21, 1989. Regulation: 8.