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C.R. Bard, Inc.
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BARD SOFT MESH, MODELS 0117001, 0117002, 0117003, 0117004, 0117005, 0117006, 0117007 is an FDA 510(k)-cleared medical device (K033814) manufactured by C.R. Bard, 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 February 29, 2004. Regulation: 8.