DHD METERED DOSE INHALER (MDI) SPACER (MODIFICATION)

DHD METERED DOSE INHALER (MDI) SPACER (MODIFICATION) is an FDA 510(k)-cleared medical device (K953206) manufactured by Dhd Diemolding Healthcare Div.. This device is classified under the Anesthesiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on August 27, 1995. Regulation: 8.