ClearanceBrief
510(k) K090730 ยท CAF Nebulizer (Direct Patient Interface)

AKITA JET

ApplicantActivaero America, Inc., Bonita Springs FL, US
DecisionSubstantially Equivalent, Nov 13, 2009
ReceivedMar 19, 2009
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K090730

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.