ClearanceBrief
510(k) K031908 ยท CAF Nebulizer (Direct Patient Interface)

MED2000 SPA NEBULIZER COMPRESSORS, MODELS P1 AND P2, WITH NEBULIZER, AND MED2000 SPA NEBULIZER, MODEL A1/C (ANDYFLOW)

ApplicantMed2000 S.R.L., Great Neck NY, US
DecisionSubstantially Equivalent, Jan 14, 2004
ReceivedJun 20, 2003
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K031908

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.