LAPAROSCOPY DRAPE, BOUNDARY

LAPAROSCOPY DRAPE, BOUNDARY is an FDA 510(k)-cleared medical device (K772301) manufactured by Procter & Gamble Mfg. Co.. This device is classified under the General, Plastic Surgery specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on December 19, 1977. Regulation: 8.