510(k) K001224 ยท FGE Stents, Drains And Dilators For The Biliary Ducts
RX HERCULINK 14 BILIARY STENT SYSTEM, MODELS 1005127-13, 1005129-13, 1005131-13, 1005133-13, 1005135-13, 1005137-13, 100
| Applicant | Guidant Corp., Santa Clara CA, US |
| Decision | Unknown, May 17, 2000 |
| Received | Apr 17, 2000 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K001224
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.