ClearanceBrief
510(k) K143719 ยท CAF Nebulizer (Direct Patient Interface)

Aeroneb USB Contoller System

ApplicantAerogen Limited, Galway, IE
DecisionSubstantially Equivalent, Jul 10, 2015
ReceivedDec 29, 2014
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K143719

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.