
American Bantex Corp.
Free shipping on orders over $99 · 30-day returns
AMERICAN BANTEX HUMIDIFIER, DRY, BUBBLE, MODELS B9000, 3 PSI AND B9100, 6 PSI is an FDA 510(k)-cleared medical device (K041963) manufactured by American Bantex Corp.. This device is classified under the Anesthesiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on October 19, 2004. Regulation: 8.