HORIZON 1 AND 2 PROGRAMABLE FULL SHELL AND IN THE CANAL

HORIZON 1 AND 2 PROGRAMABLE FULL SHELL AND IN THE CANAL is an FDA 510(k)-cleared medical device (K963607) 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 19, 1996. Regulation: 8.