RESPIR THER HUMID CONTAIN STERILE WATER FOR USP

RESPIR THER HUMID CONTAIN STERILE WATER FOR USP is an FDA 510(k)-cleared medical device (K853146) manufactured by Automatic Liquid Packaging, 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 5, 1985. Regulation: 8.