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Kci USA, Inc.
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V.A.C. THERAPY SYSTEMS-ACTI V.A.C. THERAPY UNIT MODEL# 340000 is an FDA 510(k)-cleared medical device (K063692) manufactured by Kci USA, 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 6, 2007. Regulation: 8.