ClearanceBrief
510(k) K223120 ยท CBK Ventilator, Continuous, Facility Use

Ventoux VC2; Ventoux VC3

ApplicantFlight Medical Innovations , Ltd., Petach Tikva, IL
DecisionSubstantially Equivalent, Dec 2, 2024
ReceivedOct 3, 2022
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K223120

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.