TTECH MODEL 200E + TENS DEVICE

TTECH MODEL 200E + TENS DEVICE is an FDA 510(k)-cleared medical device (K021436) manufactured by Theratech, 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 July 29, 2002. Regulation: 8.