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Surgical Laser Technologies, Inc.
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SLT VENOUS FIBER DELIVERY SYSTEMS, MODEL: 0041-6772/0041-6781/0041-6752/0041-6761/0041-6912/0041-6921 is an FDA 510(k)-cleared medical device (K023624) manufactured by Surgical Laser Technologies, 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 January 26, 2003. Regulation: 8.