510(k) K241453 ยท QWH Prognostic Test For Development Or Progression Of Preeclampsia
Elecsys sFlt-1 and Elecsys PlGF
| Applicant | Roche Diagnostics, Indianapolis IN, US |
| Decision | Substantially Equivalent, Feb 7, 2025 |
| Received | May 22, 2024 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K241453
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.