510(k) K041032 ยท FGE Stents, Drains And Dilators For The Biliary Ducts
MODIFICATION TO LIFESTENT SDS AND XL SDS BILIARY ENDOPROSTHESIS
| Applicant | Orbus Medical Technologies, Fort Lauderdale FL, US |
| Decision | Unknown, May 10, 2004 |
| Received | Apr 21, 2004 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K041032
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.