ClearanceBrief
510(k) K943990 ยท CAF Nebulizer (Direct Patient Interface)

3000 AEROSOL TWO

ApplicantMedical Industries America, Inc., Adel IA, US
DecisionSubstantially Equivalent, Mar 21, 1995
ReceivedAug 16, 1994
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K943990

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.