510(k) K990808 ยท FGE Stents, Drains And Dilators For The Biliary Ducts
PBN DILATORS
| Applicant | Medical Device Technologies, Inc., Gainesville FL, US |
| Decision | Substantially Equivalent, Nov 26, 1999 |
| Received | Mar 11, 1999 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K990808
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.