510(k) K141344 ยท FAD Stent, Ureteral
EXPEL NEPHROURETERAL DRAINAGE STENT WITH TWIST-LOC HUB SYSTEM, EXPEL URETERAL DRAINAGE STENT SYSTEM
| Applicant | Boston Scientific Corp, Maple Grove MN, US |
| Decision | Substantially Equivalent, Oct 17, 2014 |
| Received | May 22, 2014 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K141344
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.