COMPRESSOR/NEBULIZER #3650

COMPRESSOR/NEBULIZER #3650 is an FDA 510(k)-cleared medical device (K970289) manufactured by Devilbiss Health Care, 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 April 14, 1997. Regulation: 8.