INS - T.E.N.S.

INS - T.E.N.S. is an FDA 510(k)-cleared medical device (K770448) manufactured by Stimulation Technology, 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 March 14, 1977. Regulation: 8.