XBO1-824-18/19/20 BIOPSY FORCEPS

XBO1-824-18/19/20 BIOPSY FORCEPS is an FDA 510(k)-cleared medical device (K012074) manufactured by The Olympus Optical Co.. This device is classified under the Gastroenterology, Urology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on September 24, 2001. Regulation: 8.