PHONAK PICONET 232X-AZ BTE HEARING INSTRUMENT

PHONAK PICONET 232X-AZ BTE HEARING INSTRUMENT is an FDA 510(k)-cleared medical device (K935791) 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 January 25, 1994. Regulation: 8.