TECA NEUROPTO WITH OS-5 STIMULATOR

TECA NEUROPTO WITH OS-5 STIMULATOR is an FDA 510(k)-cleared medical device (K861069) manufactured by Teca, 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 January 26, 1987. Regulation: 8.