3-DAY RELEASE OF ETHYLENE OXIDE DEVICE

3-DAY RELEASE OF ETHYLENE OXIDE DEVICE is an FDA 510(k)-cleared medical device (K832352) manufactured by Parke-Davis Co.. This device is classified under the Anesthesiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on January 12, 1984. Regulation: 8.