eRapid Nebulizer System

eRapid Nebulizer System is an FDA 510(k)-cleared medical device (K223840) manufactured by Pari Respiratory Equipment, 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 August 10, 2023. Regulation: 8.