PREEMICARE NEBUTECH NEBULIZER SYSTEM

PREEMICARE NEBUTECH NEBULIZER SYSTEM is an FDA 510(k)-cleared medical device (K896375) manufactured by Preemicare 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 October 28, 1990. Regulation: 8.