KEISEI SCALPEL (STERILE AND NON-STERILE)

KEISEI SCALPEL (STERILE AND NON-STERILE) is an FDA 510(k)-cleared medical device (K863213) manufactured by Keisei Medical Industrial Co., Ltd.. This device is classified under the General, Plastic Surgery specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on September 1, 1986. Regulation: 8.