RETeval Visual Electrodiagnostic Device

RETeval Visual Electrodiagnostic Device is an FDA 510(k)-cleared medical device (K142567) manufactured by Lkc Technologies, 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 May 18, 2015. Regulation: 8.