510(k) K880660 ยท FAD Stent, Ureteral
SURGITEK SUPER DOUBLE J URETERAL STENT KIT
| Applicant | Surgitek, Racine WI, US |
| Decision | Substantially Equivalent, Apr 14, 1988 |
| Received | Feb 17, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K880660
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.