510(k) K162979 ยท FJL Resectoscope
Veloxion System
| Applicant | Corinth Medtech, Inc., Cupertino CA, US |
| Decision | Substantially Equivalent, Mar 24, 2017 |
| Received | Oct 26, 2016 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K162979
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.