MODEL 52 BUNN DRY AIR SUPPLY

MODEL 52 BUNN DRY AIR SUPPLY is an FDA 510(k)-cleared medical device (K800534) manufactured by Greene & Kellogg, 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 March 24, 1980. Regulation: 8.