510(k) K021824 ยท FGE Stents, Drains And Dilators For The Biliary Ducts
DYNALINK .035 BILIARY SELF-EXPANDING STENT SYSTEM, MODELS 1010102-38,1010102-56,1010102-80,1010103-38,1010103-56, 101010
| Applicant | Guidant Corp., Menlo Park CA, US |
| Decision | Unknown, Jul 2, 2002 |
| Received | Jun 4, 2002 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K021824
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.