ClearanceBrief
510(k) K962872 ยท CAF Nebulizer (Direct Patient Interface)

RESPIFLO

ApplicantTyco Healthcare Deutschaland GmbH, Neustadt A D Donau, DE
DecisionUnknown, Feb 25, 1997
ReceivedJul 23, 1996
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K962872

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.