EFLOW ELECTRONIC INHALER/NEBULIZER

EFLOW ELECTRONIC INHALER/NEBULIZER is an FDA 510(k)-cleared medical device (K033833) manufactured by Pari Innovative Manufacturers, Inc.. This device is classified under the Anesthesiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on May 4, 2004. Regulation: 8.