A&D UN-231 ULTRASONIC HANDY NEBULIZER

A&D UN-231 ULTRASONIC HANDY NEBULIZER is an FDA 510(k)-cleared medical device (K941627) manufactured by A & D Corporate. This device is classified under the Anesthesiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on December 27, 1995. Regulation: 8.