ClearanceBrief
510(k) K014056 ยท CAF Nebulizer (Direct Patient Interface)

SALTER LABS MODIFIED NEBUTECH NEBULIZER

ApplicantSalter Labs, Arvin CA, US
DecisionSubstantially Equivalent, Feb 1, 2002
ReceivedDec 10, 2001
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K014056

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.