ClearanceBrief
510(k) K935693 ยท CAF Nebulizer (Direct Patient Interface)

AUTONEB BREATH ACTUATED CONTROLLER AND ACCESSORY KIT

ApplicantVortran Medical Technology 1, Inc., Sacramento CA, US
DecisionSubstantially Equivalent, Aug 25, 1994
ReceivedNov 29, 1993
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K935693

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.