510(k) K233380 ยท JAA System, X-Ray, Fluoroscopic, Image-Intensified
TRIDENT Mobile Fluoroscopy System
| Applicant | Dornier Medtech America, Kennesaw GA, US |
| Decision | Substantially Equivalent, Jun 26, 2024 |
| Received | Oct 2, 2023 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K233380
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.