510(k) K200022 ยท OWB Interventional Fluoroscopic X-Ray System
FLUSION-9001, Fluoroscopic C-arm Mobile X-ray System
| Applicant | Livermoretech, Inc., Plano TX, US |
| Decision | Substantially Equivalent, Apr 3, 2020 |
| Received | Jan 6, 2020 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K200022
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.