510(k) K030503 ยท FAD Stent, Ureteral
MODIFICATION TO CONTOUR POLARIS URETERAL STENT
| Applicant | Boston Scientific Corp, Natick, MA, US |
| Decision | Substantially Equivalent, Mar 17, 2003 |
| Received | Feb 19, 2003 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K030503
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.