510(k) K233230 · OWB Interventional Fluoroscopic X-Ray System
See Factor CT3
| Applicant | Epica International, Inc., Duncan SC, US |
| Decision | Substantially Equivalent, Jun 21, 2024 |
| Received | Sep 28, 2023 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K233230
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.