HOLDEN-WALKER HUMIDIFIER-NEBULIZER KIT

HOLDEN-WALKER HUMIDIFIER-NEBULIZER KIT is an FDA 510(k)-cleared medical device (K963917) manufactured by Holden Walker Corp.. This device is classified under the Anesthesiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on February 24, 1997. Regulation: 8.