Pulmonx Corporation
FDA 510(k) & PMA Approved Devices — 4 products
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Total Devices4
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K253096 | Chartis Precision Catheter | CBI | 2026-02-13 | View |
| 510(k) | K222340 | Chartis Precision Catheter | CBI | 2022-12-01 | View |
| 510(k) | K212494 | Lung Image Analysis | JAK | 2021-09-02 | View |
| 510(k) | K180011 | Pulmonx Chartis Tablet Console | BZG | 2018-07-13 | View |
No matching devices.
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