ULTRASONIC NEBULISER MODEL 2010

ULTRASONIC NEBULISER MODEL 2010 is an FDA 510(k)-cleared medical device (K072136) manufactured by Wilfred Kromker GmbH. This device is classified under the Anesthesiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on July 14, 2008. Regulation: 8.