HYDROCISION ARTHROJET SYSTEM WITH CAUTERY

HYDROCISION ARTHROJET SYSTEM WITH CAUTERY is an FDA 510(k)-cleared medical device (K993009) manufactured by Hydrocision, Inc.. This device is classified under the Orthopedic specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on October 24, 1999. Regulation: 8.