
Woodside Biomedical, Inc.
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RELIEFBAND DEVICE, MODELS RB-DL, RB-EL, RB-RL is an FDA 510(k)-cleared medical device (K020180) manufactured by Woodside Biomedical, 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 20, 2002. Regulation: 8.