DEY VIAL SODIUM CHLORIDE 3%

DEY VIAL SODIUM CHLORIDE 3% is an FDA 510(k)-cleared medical device (K972778) manufactured by Dey Laboratories, Inc.. This device is classified under the Anesthesiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on October 7, 1997. Regulation: 8.