THYMATRON 2000 ELECTROCONVULSIVE SYSTEM

THYMATRON 2000 ELECTROCONVULSIVE SYSTEM is an FDA 510(k)-cleared medical device (K945120) manufactured by Somatics, 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 October 25, 1995. Regulation: 8.