510(k) K914699 ยท FGE Stents, Drains And Dilators For The Biliary Ducts
URESIL FIXATION DEVICE
| Applicant | Uresil Corp., Skokie IL, US |
| Decision | Substantially Equivalent, Feb 19, 1992 |
| Received | Oct 18, 1991 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K914699
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.