BTE SUPER-FRONT PPCL4, SUPER-FRONT PPC4

BTE SUPER-FRONT PPCL4, SUPER-FRONT PPC4 is an FDA 510(k)-cleared medical device (K900830) manufactured by Phonak, Inc.. This device is classified under the Ear, Nose, Throat specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on May 22, 1990. Regulation: 8.