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Molnlycke Health Care
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KLINIDRAPE SURGICAL DRAPES is an FDA 510(k)-cleared medical device (K031131) manufactured by Molnlycke Health Care. 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 9, 2003. Regulation: 8.