REPROCESSED RESTEP COMPRESSION SLEEVES

REPROCESSED RESTEP COMPRESSION SLEEVES is an FDA 510(k)-cleared medical device (K101087) manufactured by Ascent Heatlhcare Solutions. This device is classified under the Cardiovascular specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on July 15, 2010. Regulation: 8.