SURGICAL DRAPES AND ACCESSORIES USING PEBAX FILM

SURGICAL DRAPES AND ACCESSORIES USING PEBAX FILM is an FDA 510(k)-cleared medical device (K870124) manufactured by Avery Intl.. 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 3, 1987. Regulation: 8.