PROPPER EO LINE ETHYLENE OXIDE STERILIZATION INTEGRATOR

PROPPER EO LINE ETHYLENE OXIDE STERILIZATION INTEGRATOR is an FDA 510(k)-cleared medical device (K973585) manufactured by Propper Mfg. Co., 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 November 5, 1998. Regulation: 8.