REPROCESSED HOT BIOPSY FORCEPS

REPROCESSED HOT BIOPSY FORCEPS is an FDA 510(k)-cleared medical device (K050136) manufactured by Sterilmed, 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 July 19, 2005. Regulation: 8.