510(k) K993588 ยท FGE Stents, Drains And Dilators For The Biliary Ducts
MODIFICATION TO RX HERCULINK 14 BILIARY STENT SYSTEM, MODELS 1005126-13, 1005128-13, 1005130-13, 1005132-13, 1005134-13,
| Applicant | Guidant Corp., Santa Clara CA, US |
| Decision | Substantially Equivalent, Nov 17, 1999 |
| Received | Oct 22, 1999 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K993588
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.