510(k) K212873 ยท MUE Full Field Digital, System, X-Ray, Mammographic
Aspire Cristalle
| Applicant | Fujifilm Corporation, Ashigara Kami-Gun, JP |
| Decision | Substantially Equivalent, May 27, 2022 |
| Received | Sep 9, 2021 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K212873
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.