510(k) K923096 ยท FGE Stents, Drains And Dilators For The Biliary Ducts
URESIL BILLIARY CATHETER
| Applicant | Uresil Corp., Skokie IL, US |
| Decision | Substantially Equivalent, Jul 13, 1993 |
| Received | Jun 25, 1992 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K923096
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.