K223120
- 510(k) number
- K223120
- Device name
- Ventoux VC2; Ventoux VC3
- Applicant
- Flight Medical Innovations , Ltd. IL
- Product code
- CBK — Ventilator, Continuous, Facility Use
- Decision date
- 2024-12-02
- Date received
- 2022-10-03
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Anesthesiology
PDFDownload 510(k) SummaryArchived here · 1.2 MB · U.S. public domain
Also available from FDA: K223120.pdf
Official FDA record: K223120
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.