HYGIA HEALTH SERVICES REPROCESSED NUTECH FOOT WRAP

HYGIA HEALTH SERVICES REPROCESSED NUTECH FOOT WRAP is an FDA 510(k)-cleared medical device (K012650) manufactured by Hygia Health Services, Inc.. This device is classified under the Cardiovascular specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on April 11, 2002. Regulation: 8.