CHALLENGER HOT BIOPSY FORCEPS

CHALLENGER HOT BIOPSY FORCEPS is an FDA 510(k)-cleared medical device (K860366) manufactured by Microvasive. 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 April 6, 1986. Regulation: 8.