510(k) K941952 ยท FAD Stent, Ureteral
SURGITEK INFUSER
| Applicant | Surgitek, Racine WI, US |
| Decision | Substantially Equivalent, May 24, 1994 |
| Received | Apr 22, 1994 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K941952
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.