ELECTRO-GONIOMETER DIAGNOSTIC DEVICE

ELECTRO-GONIOMETER DIAGNOSTIC DEVICE is an FDA 510(k)-cleared medical device (K901290) manufactured by Chattanooga Group, Inc.. This device is classified under the Orthopedic specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on September 30, 1990. Regulation: 8.