PROBE, COAGULATION ACCESSORY

PROBE, COAGULATION ACCESSORY is an FDA 510(k)-cleared medical device (K772220) 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 December 12, 1977. Regulation: 8.