510(k) K200260 ยท FAD Stent, Ureteral
Percuflex Ureteral Stent System, Percuflex Ureteral Stent System Kit, Percuflex Nephroureteral Stent System, Amplatz Anchor Catheter System
| Applicant | Boston Scientific Corporation, Maple Grove MN, US |
| Decision | Unknown, Apr 26, 2021 |
| Received | Feb 3, 2020 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K200260
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.