KLINIDRAPE SURGICAL DRAPES

KLINIDRAPE SURGICAL DRAPES is an FDA 510(k)-cleared medical device (K000906) manufactured by Molnlycke Health Care, Inc.. 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 June 22, 2000. Regulation: 8.