ClearanceBrief
510(k) K913326 ยท CAF Nebulizer (Direct Patient Interface)

DHD METERED DOSE INHALER (MDI) SPACER

ApplicantDhd Diemolding Healthcare Div., Canastota NY, US
DecisionSubstantially Equivalent, Jan 7, 1992
ReceivedJul 25, 1991
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K913326

No recall in the FDA data names this 510(k).

Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.