510(k) K161277 ยท FAD Stent, Ureteral
ConvertX Nephroureteral Stent System
| Applicant | Brightwater Medical, Dunlap IL, US |
| Decision | Substantially Equivalent, Nov 22, 2016 |
| Received | May 6, 2016 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K161277
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.