TECA MODEL-10 ELECTROMYOGRAPH

TECA MODEL-10 ELECTROMYOGRAPH is an FDA 510(k)-cleared medical device (K802637) manufactured by Teca, Inc.. This device is classified under the Physical Medicine specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on November 25, 1980. Regulation: 8.