K AMP FULL SHELL AND IN THE EAR

K AMP FULL SHELL AND IN THE EAR is an FDA 510(k)-cleared medical device (K953729) manufactured by Midwest City Hearing Aid Center. This device is classified under the Ear, Nose, Throat specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on September 11, 1995. Regulation: 8.