510(k) K171603 ยท FAD Stent, Ureteral
Cope Nephroureterostomy Stent and Amplatz Ureteral Stent Set
| Applicant | Cook Incorporated, Bloomington IN, US |
| Decision | Unknown, Apr 16, 2018 |
| Received | Jun 1, 2017 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K171603
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.