PARE ENDOSCOPIC SUTURING SYSTEM

PARE ENDOSCOPIC SUTURING SYSTEM is an FDA 510(k)-cleared medical device (K003102) manufactured by Pare Surgical, 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 February 26, 2001. Regulation: 8.