510(k) K852389 ยท FAD Stent, Ureteral
URETERAL STENT
| Applicant | American Medical Systems, Inc., Minnetonka MN, US |
| Decision | Substantially Equivalent, Sep 5, 1985 |
| Received | Jun 5, 1985 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K852389
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.