ClearanceBrief
510(k) K080926 ยท CAF Nebulizer (Direct Patient Interface)

AEROECLIPSE DURABLE BREATH ACTUATED NEBULIZER

ApplicantTrudell Medical Intl., London, CA
DecisionSubstantially Equivalent, Aug 12, 2008
ReceivedApr 2, 2008
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K080926

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.