FDA 510(k) Applications Submitted by Pulmonx Corporation
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K222340 | 08/03/2022 | Chartis Precision Catheter | Pulmonx Corporation |
| K180011 | 01/02/2018 | Pulmonx Chartis Tablet Console | Pulmonx Corporation |
| K212494 | 08/09/2021 | Lung Image Analysis | Pulmonx Corporation |
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