ClearanceBrief
510(k) K912566 ยท CAF Nebulizer (Direct Patient Interface)

MINITROP AEROSOL UNIT

ApplicantHeyer America, Inc., Washington DC, US
DecisionSubstantially Equivalent, Aug 20, 1991
ReceivedJun 11, 1991
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K912566

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.