510(k) K201436 ยท FAD Stent, Ureteral
Vortek Single Loop Ureteral Stent
| Applicant | Coloplast Corp., Plymouth MN, US |
| Decision | Substantially Equivalent, Feb 25, 2021 |
| Received | Jun 1, 2020 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K201436
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.