510(k) K222340 ยท CBI Tube, Tracheal/Bronchial, Differential Ventilation (W/Wo Connector)
Chartis Precision Catheter
| Applicant | Pulmonx Corporation, Redwood City CA, US |
| Decision | Substantially Equivalent, Dec 1, 2022 |
| Received | Aug 3, 2022 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K222340
No recall in the FDA data names this 510(k).
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.