K253096
- 510(k) number
- K253096
- Device name
- Chartis Precision Catheter
- Applicant
- Pulmonx Corporation CA · US
- Product code
- CBI — Tube, Tracheal/Bronchial, Differential Ventilation (
- Decision date
- 2026-02-13
- Date received
- 2025-09-23
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Anesthesiology
PDFDownload 510(k) SummaryArchived here · 0.4 MB · U.S. public domain
Also available from FDA: K253096.pdf
Official FDA record: K253096
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.