510(k) K990854 ยท FGE Stents, Drains And Dilators For The Biliary Ducts
INNERDYNE RADIALLY EXPANDING DILATION, RED DEVICE
| Applicant | Innerdyne, Inc., Salt Lake City UT, US |
| Decision | Substantially Equivalent, Aug 2, 1999 |
| Received | Mar 15, 1999 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K990854
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.