ClearanceBrief
510(k) K874041 ยท CAF Nebulizer (Direct Patient Interface)

DEVILBISS MODEL 8500D

ApplicantThe Devilbiss Co., Somerset PA, US
DecisionSubstantially Equivalent, Dec 23, 1987
ReceivedOct 5, 1987
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K874041

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.