RUDD-CLINIC HEMORRHOIDAL FORCEPS

RUDD-CLINIC HEMORRHOIDAL FORCEPS is an FDA 510(k)-cleared medical device (K800441) manufactured by J. Sklar Mfg. Co., Inc.. This device is classified under the Gastroenterology, Urology specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on April 7, 1980. Regulation: 8.