510(k) K191341 ยท FJL Resectoscope
Veloxion Controller Kit, Veloxion Fluid Control Set, Veloxion Resectoscope, Veloxion Video Control Unit, Veloxion Roll Stand, Waste Management Tubing, Tissue Catch, Waste Management Bags
| Applicant | Corinth Medtech, Inc., Cupertino CA, US |
| Decision | Substantially Equivalent, Jun 13, 2019 |
| Received | May 20, 2019 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K191341
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.