STERILOX LIQUID CHEMICAL STERILANT SYSTEM

STERILOX LIQUID CHEMICAL STERILANT SYSTEM is an FDA 510(k)-cleared medical device (K013280) manufactured by Sterilox Technologies, Inc.. This device is classified under the General Hospital specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on September 17, 2002. Regulation: 8.