RELIEFBAND TENS UNIT (MODIFICATION)

RELIEFBAND TENS UNIT (MODIFICATION) is an FDA 510(k)-cleared medical device (K961050) 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 July 31, 1997. Regulation: 8.