KIMBERLY-CLARK PROCEDURE GOWN

KIMBERLY-CLARK PROCEDURE GOWN is an FDA 510(k)-cleared medical device (K052824) manufactured by Kimberly-Clark Corp.. This device is classified under the General, Plastic Surgery specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on May 1, 2006. Regulation: 8.