SUTURE REMOVAL WOUND CLOSURE-INSTRU-

SUTURE REMOVAL WOUND CLOSURE-INSTRU- is an FDA 510(k)-cleared medical device (K834367) manufactured by Sterling Multi-Products, Inc.. This device is classified under the General, Plastic Surgery specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on May 29, 1984. Regulation: 8.