PREFILLED RESPIRATORY THERAPY VIAL

PREFILLED RESPIRATORY THERAPY VIAL is an FDA 510(k)-cleared medical device (K830943) 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 April 27, 1983. Regulation: 8.