ClearanceBrief
510(k) K982043 ยท CAF Nebulizer (Direct Patient Interface)

BRENEB

ApplicantBremed Italia, S.R.L., Arnold MO, US
DecisionSubstantially Equivalent, Nov 9, 1998
ReceivedJun 10, 1998
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K982043

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.