RELIEF BAND (T.E.N.S. DEVICE)

RELIEF BAND (T.E.N.S. DEVICE) is an FDA 510(k)-cleared medical device (K901704) manufactured by Maven Labs, 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 November 18, 1991. Regulation: 8.