MEDIVISION ARTHROSCOP

MEDIVISION ARTHROSCOP is an FDA 510(k)-cleared medical device (K971996) manufactured by Medivision Scope Service Center, 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 July 30, 1997. Regulation: 8.