Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

Pulmonx Corporation

FDA 510(k) & PMA Approved Devices — 5 products

Total Devices5
Categories4
Latest FDA decision2026-06-17
TypeNumberDevice NameCodeDateActions
PMA P180002 Valve, pulmonaryNJK2026-06-17 View
510(k) K253096 Chartis Precision CatheterCBI2026-02-13 View
510(k) K222340 Chartis Precision CatheterCBI2022-12-01 View
510(k) K212494 Lung Image AnalysisJAK2021-09-02 View
510(k) K180011 Pulmonx Chartis Tablet ConsoleBZG2018-07-13 View
↑