ClearanceBrief
510(k) K833922 ยท CAF Nebulizer (Direct Patient Interface)

BRETHANCER, DRUG DELIVERY SYS-INHAL

ApplicantCiba-Geigy Corp., Walker MI, US
DecisionSubstantially Equivalent, Dec 8, 1983
ReceivedNov 14, 1983
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K833922

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.