510(k) K170362 ยท FAD Stent, Ureteral
VORTEK HYDRO-COATED DOUBLE LOOP URETERAL STENTS
| Applicant | Coloplast Corp., Plymouth MN, US |
| Decision | Substantially Equivalent, Nov 15, 2017 |
| Received | Feb 6, 2017 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K170362
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.