TELEX SELECT 1-40 WITH ADAPTIVE COMPRESSION

TELEX SELECT 1-40 WITH ADAPTIVE COMPRESSION is an FDA 510(k)-cleared medical device (K982683) manufactured by Telex Communications, Inc.. This device is classified under the Ear, Nose, Throat specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on October 5, 1998. Regulation: 8.