510(k) K180011 ยท BZG Spirometer, Diagnostic
Pulmonx Chartis Tablet Console
| Applicant | Pulmonx Corporation, Redwood City CA, US |
| Decision | Substantially Equivalent, Jul 13, 2018 |
| Received | Jan 2, 2018 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K180011
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.