510(k) K222998 ยท OWB Interventional Fluoroscopic X-Ray System
F3
| Applicant | Acrew Imaging, Inc., Ocean View DE, US |
| Decision | Substantially Equivalent, Jun 20, 2023 |
| Received | Sep 28, 2022 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K222998
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.