LIDO(TM) WORKSET

LIDO(TM) WORKSET is an FDA 510(k)-cleared medical device (K880018) manufactured by Loredan Biomedical, Inc.. This device is classified under the Physical Medicine specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on February 25, 1988. Regulation: 8.