KARL STORZ TRACHEAL HIGH FREQUENCY RESECTOSCOPE

KARL STORZ TRACHEAL HIGH FREQUENCY RESECTOSCOPE is an FDA 510(k)-cleared medical device (K951826) manufactured by KARL STORZ Endoscopy-America, 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 May 14, 1995. Regulation: 8.