Medline ReNewal Reprocessed Compression Limb Sleeves

Medline ReNewal Reprocessed Compression Limb Sleeves is an FDA 510(k)-cleared medical device (K143166) manufactured by Surgical Instrument Service and Savings (Dba Medline Renewal. This device is classified under the Cardiovascular specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on January 15, 2015. Regulation: 8.