510(k) K800109 ยท FAD Stent, Ureteral
SURGITEK URINARY DIVERSION STENT
| Applicant | Medical Engineering Corp., Mchenry IL, US |
| Decision | Substantially Equivalent, Feb 26, 1980 |
| Received | Jan 16, 1980 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K800109
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.