510(k) K180057 ยท FAD Stent, Ureteral
VORTEK URETERAL DOUBLE LOOP STENT
| Applicant | Coloplast Corp., Plymouth MN, US |
| Decision | Substantially Equivalent, Mar 9, 2018 |
| Received | Jan 8, 2018 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K180057
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.