ClearanceBrief
510(k) K942444 ยท CAF Nebulizer (Direct Patient Interface)

3002 AEROMAX

ApplicantMedical Industries America, Inc., Adel IA, US
DecisionSubstantially Equivalent, Mar 10, 1995
ReceivedMay 23, 1994
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K942444

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.