ClearanceBrief
510(k) K081650 ยท CAF Nebulizer (Direct Patient Interface)

AERONEB GO NEBULIZER

ApplicantAerogen (Ireland), Ltd., Dangan Galway, IE
DecisionSubstantially Equivalent, Oct 23, 2008
ReceivedJun 12, 2008
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K081650

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.