510(k) K023308 ยท FGE Stents, Drains And Dilators For The Biliary Ducts
LIFESTENT SDS BILIARY ENDOPROSTHESIS, LIFESTENT XL SDS BILIARY ENDOPROSTHESIS
| Applicant | Orbus Medical Technologies, Fort Lauderdale FL, US |
| Decision | Unknown, Apr 14, 2003 |
| Received | Oct 3, 2002 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K023308
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.