510(k) K230205 ยท FJL Resectoscope
Veloxion System
| Applicant | Corinth Medtech, Inc., San Jose CA, US |
| Decision | Substantially Equivalent, Feb 24, 2023 |
| Received | Jan 25, 2023 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K230205
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.