510(k) K213186 ยท FAD Stent, Ureteral
NovoFlow Reinforced Ureteral Stent
| Applicant | Coloplast Corp., Plymouth MN, US |
| Decision | Unknown, Feb 16, 2022 |
| Received | Sep 29, 2021 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K213186
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.