510(k) K833782 ยท FAD Stent, Ureteral
SURGITEK ALL SILICONE INFECTION DOUBJ
| Applicant | Surgitek, Mchenry IL, US |
| Decision | Substantially Equivalent, Apr 2, 1984 |
| Received | Oct 28, 1983 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K833782
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.