510(k) K231776 ยท QMA Blood Collection Device For Cell-Free Nucleic Acid
Cell-Free DNA BCT
| Applicant | Streck, Inc., La Vista NE, US |
| Decision | Substantially Equivalent, Jul 26, 2024 |
| Received | Jun 16, 2023 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K231776
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.