NEBULIZER, HANDHELD (T UP-DRAFT)

NEBULIZER, HANDHELD (T UP-DRAFT) is an FDA 510(k)-cleared medical device (K760489) manufactured by Hudson Oxygen Therapy Sales Co.. This device is classified under the Anesthesiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on September 2, 1976. Regulation: 8.