WFSI'S REPROCESSED COMPRESSION SLEEVE DEVICES

WFSI'S REPROCESSED COMPRESSION SLEEVE DEVICES is an FDA 510(k)-cleared medical device (K033615) manufactured by Wheaton Franciscan Services Inc., Supply Chain. This device is classified under the Cardiovascular specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on February 12, 2004. Regulation: 8.