
Veratex Corp.
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STERILE DRAPE 17X18 W/3 FENESTRATION is an FDA 510(k)-cleared medical device (K801033) manufactured by Veratex Corp.. 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 May 19, 1980. Regulation: 8.