ClearanceBrief
510(k) K030374 ยท CAF Nebulizer (Direct Patient Interface)

SONIK LDI 20 AIR

ApplicantEvit Labs, Inc., Mcclellan CA, US
DecisionSubstantially Equivalent, Aug 25, 2003
ReceivedFeb 4, 2003
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K030374

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.