510(k) K014136 ยท FGE Stents, Drains And Dilators For The Biliary Ducts
MODIFICATION TO PROTEGE SELF-EXPANDING NITINOL STENT WITH STARPORT DELIVERY TECHNOLOGY
| Applicant | Sulzer Intratherapeutics, Inc., Saint Paul MN, US |
| Decision | Unknown, Jan 17, 2002 |
| Received | Dec 17, 2001 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K014136
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.