510(k) K233946 · MOI System, Test, Immunological, Antigen, Tumor
IMMULITE® 2000 BR-MA
| Applicant | Siemens Healthcare Diagnostics Products, Ltd., Llanberis, GB |
| Decision | Substantially Equivalent, Mar 13, 2024 |
| Received | Dec 14, 2023 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K233946
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.