
Becton, Dickinson and Co.
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BD VISIDRAPE OPHTHALMIC DRAPES; BD VISIFLEX INCISE DRAPE is an FDA 510(k)-cleared medical device (K010572) manufactured by Becton, Dickinson and Co.. 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 March 11, 2001. Regulation: 8.