RITE-BITE BIOPSY FORCEPS

RITE-BITE BIOPSY FORCEPS is an FDA 510(k)-cleared medical device (K951048) manufactured by Mill-Rose Laboratory. This device is classified under the Gastroenterology, Urology specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on March 14, 1995. Regulation: 8.