510(k) K972582 ยท FGE Stents, Drains And Dilators For The Biliary Ducts
URESIL GUIDEWIRE
| Applicant | Uresil Corp., Skokie IL, US |
| Decision | Substantially Equivalent, Nov 21, 1997 |
| Received | Jul 10, 1997 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K972582
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.