510(k) K013784 ยท FAD Stent, Ureteral
URETERAL STENT
| Applicant | Boston Scientific Corp, Natick, MA, US |
| Decision | Substantially Equivalent, Aug 8, 2002 |
| Received | Nov 14, 2001 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K013784
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.