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C.R. Bard, Inc.
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BARD CRURASOFT PATCH, MODELS 0116003 & 0116001 is an FDA 510(k)-cleared medical device (K022350) 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 August 22, 2002. Regulation: 8.