GIP/MEDI-GLOBE BIOPSY FORCEPS

GIP/MEDI-GLOBE BIOPSY FORCEPS is an FDA 510(k)-cleared medical device (K941359) manufactured by Medi-Globe Corp.. This device is classified under the Gastroenterology, Urology specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on July 11, 1994. Regulation: 8.