BRIOX MODEL 2000-C COMPRESSOR UNIT

BRIOX MODEL 2000-C COMPRESSOR UNIT is an FDA 510(k)-cleared medical device (K791240) manufactured by Briox Technologies, Inc.. This device is classified under the General, Plastic Surgery specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on July 23, 1979. Regulation: 8.