SIEMENS MODEL 284 PP-AGC

SIEMENS MODEL 284 PP-AGC is an FDA 510(k)-cleared medical device (K893574) manufactured by Siemens Hearing Instruments, 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 20, 1990. Regulation: 8.