GDC PATIENT RETURN ELECTTRODE MODEL 45021

GDC PATIENT RETURN ELECTTRODE MODEL 45021 is an FDA 510(k)-cleared medical device (K963307) manufactured by Target Therapeutics. This device is classified under the Neurology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on December 16, 1996. Regulation: 8.