
Davol Inc., Sub. C. R. Bard, Inc.
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BARD PERFIX LIGHT PLUG, MODELS 0117050, 0117060, 0117070, 0117080, 0117150, 0117160 is an FDA 510(k)-cleared medical device (K092032) manufactured by Davol Inc., Sub. 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 December 7, 2009. Regulation: 8.