CORDIS BIPAL 7 BIOPSY FORCEPS

CORDIS BIPAL 7 BIOPSY FORCEPS is an FDA 510(k)-cleared medical device (K920289) 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 March 29, 1992. Regulation: 8.