ETI BIPOLAR HEMOSTATIC PROBE

ETI BIPOLAR HEMOSTATIC PROBE is an FDA 510(k)-cleared medical device (K031026) manufactured by Endo-Therapeutics, 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 June 26, 2003. Regulation: 8.