510(k) K180216 ยท FAD Stent, Ureteral
Seidmon Antegrade AQ Stent Set
| Applicant | Cook Incorporated, Bloomington IN, US |
| Decision | Substantially Equivalent, Sep 28, 2018 |
| Received | Jan 25, 2018 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K180216
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.