510(k) K180469 ยท FAD Stent, Ureteral
ImaJin Silicone Hydro-Coated Double Loop Ureteral Stent
| Applicant | Coloplast Corp., Plymouth MN, US |
| Decision | Substantially Equivalent, Nov 6, 2018 |
| Received | Feb 21, 2018 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K180469
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.