510(k) K181971 ยท FAD Stent, Ureteral
Bander Ureteral Diversion Stent Set, Dretler Ureteroscopy Stent Set
| Applicant | Cook Incorporated, Bloomington IN, US |
| Decision | Unknown, Apr 23, 2019 |
| Received | Jul 24, 2018 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K181971
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.