CORDIS BIPAL BIOPSY FORCEPS

CORDIS BIPAL BIOPSY FORCEPS is an FDA 510(k)-cleared medical device (K914567) manufactured by Cordis Corp.. This device is classified under the Cardiovascular specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on December 17, 1991. Regulation: 8.