510(k) K241891 ยท QWO Radiology Software For Referral Of Findings Related To Fibrotic Lung Disease.
ScreenDx
| Applicant | Imvaria, Inc., Berkeley CA, US |
| Decision | Substantially Equivalent, Jan 10, 2025 |
| Received | Jun 28, 2024 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K241891
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.