510(k) K130591 ยท FGE Stents, Drains And Dilators For The Biliary Ducts
SUPERA VERITAS
| Applicant | Idev Technologies, Inc., Webster TX, US |
| Decision | Unknown, May 2, 2013 |
| Received | Mar 7, 2013 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K130591
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.