DISPOS. & SPONGE FORCEPS PEAN ARTERY

DISPOS. & SPONGE FORCEPS PEAN ARTERY is an FDA 510(k)-cleared medical device (K843074) manufactured by Greene International Corp.. This device is classified under the General, Plastic Surgery specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on August 16, 1984. Regulation: 8.