SALTER LABS MODIFIED NEBUTECH NEBULIZER

SALTER LABS MODIFIED NEBUTECH NEBULIZER is an FDA 510(k)-cleared medical device (K014056) manufactured by Salter Labs. This device is classified under the Anesthesiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on January 31, 2002. Regulation: 8.