ClearanceBrief
510(k) K830943 ยท CAF Nebulizer (Direct Patient Interface)

PREFILLED RESPIRATORY THERAPY VIAL

ApplicantAutomatic Liquid Packaging, Inc., Mchenry IL, US
DecisionSubstantially Equivalent, Apr 28, 1983
ReceivedMar 24, 1983
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K830943

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.