510(k) K831446 ยท FAD Stent, Ureteral
SURGITEK NEPHROSTENT KIT
| Applicant | Mec/Surgitek Products, Mchenry IL, US |
| Decision | Substantially Equivalent, Jun 22, 1983 |
| Received | May 5, 1983 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K831446
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.