KARL STORZ ICG Imaging System

KARL STORZ ICG Imaging System is an FDA 510(k)-cleared medical device (K180146) manufactured by Karl Storz Endoscopy America, Inc.. This device is classified under the Neurology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on April 16, 2018. Regulation: 8.