CORDIS BIPAL 7 /BIOPSY & BIPAL BIOPSY FORCEPS, MODIF

CORDIS BIPAL 7 /BIOPSY & BIPAL BIOPSY FORCEPS, MODIF is an FDA 510(k)-cleared medical device (K933235) 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 January 5, 1994. Regulation: 8.