ONE INCISION BI-POLAR ELECTRO. FORCEPS

ONE INCISION BI-POLAR ELECTRO. FORCEPS is an FDA 510(k)-cleared medical device (K781089) manufactured by Kli. This device is classified under the Obstetrics/Gynecology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on July 16, 1978. Regulation: 8.