ClearanceBrief
510(k) K963910 ยท CAF Nebulizer (Direct Patient Interface)

HEART NEBULIZER #100609

ApplicantVortran Medical Technology 1, Inc., Sacramento CA, US
DecisionSubstantially Equivalent, Dec 16, 1996
ReceivedSep 30, 1996
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K963910

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.