TOWEL, DRAPE, BOUNDARY

TOWEL, DRAPE, BOUNDARY is an FDA 510(k)-cleared medical device (K780036) manufactured by Procter & Gamble Mfg. 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 January 23, 1978. Regulation: 8.