REPROCESSED SINGLE USE DEVICES BIOPSY FORCEPS

REPROCESSED SINGLE USE DEVICES BIOPSY FORCEPS is an FDA 510(k)-cleared medical device (K033593) manufactured by Clearmedical, Inc.. 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 November 19, 2003. Regulation: 8.