510(k) K262432 ยท SCA Multi-Analyte Respiratory Virus Antigen Detection Test
CorDx Tyfast Flu A/B & COVID-19 At Home Multiplex Rapid Test; CorDx Tyfast Flu A/B & COVID-19 Multiplex Rapid Test
| Applicant | CorDx, Inc., Alpharetta GA, US |
| Decision | Substantially Equivalent, Oct 14, 2026 |
| Received | Jul 16, 2026 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K262432
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.