510(k) K212956 ยท OWB Interventional Fluoroscopic X-Ray System
FDR Cross (DR-XD 3000)
| Applicant | Fujifilm Corporation, Ashigara Kami-Gun, JP |
| Decision | Substantially Equivalent, Nov 8, 2021 |
| Received | Sep 16, 2021 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K212956
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.