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Pulmonx Corporation

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
4
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K253096Chartis Precision CatheterFebruary 13, 2026
K222340Chartis Precision CatheterDecember 1, 2022
K212494Lung Image AnalysisSeptember 2, 2021
K180011Pulmonx Chartis Tablet ConsoleJuly 13, 2018