ClearanceBrief
510(k) K930949 ยท CAF Nebulizer (Direct Patient Interface)

VOYAGE

ApplicantMada Medical Products, Inc., Carlstadt NJ, US
DecisionSubstantially Equivalent, Jun 1, 1993
ReceivedFeb 23, 1993
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K930949

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.