BARD ENDOCINCH SUTURING SYSTEM # 000452; 000454; 000595

BARD ENDOCINCH SUTURING SYSTEM # 000452; 000454; 000595 is an FDA 510(k)-cleared medical device (K003956) manufactured by C.R. Bard, 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 January 4, 2001. Regulation: 8.