MICROCIRRUS MEDICAL NEBULIZER

MICROCIRRUS MEDICAL NEBULIZER is an FDA 510(k)-cleared medical device (K881935) manufactured by Dhd Medical Products Div. Diemolding 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 June 21, 1988. Regulation: 8.