510(k) K172471 ยท DEH Lambda, Antigen, Antiserum, Control
VENTANA CD30 (Ber-H2) RxDx Assay
| Applicant | Ventana Medical Systems, Inc., Tucson AZ, US |
| Decision | Substantially Equivalent, May 8, 2018 |
| Received | Aug 15, 2017 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K172471
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.