510(k) K913928 ยท FAD Stent, Ureteral
SURGITEK(R) 4.5FR LUBRI-FLEX(TM) URETERAL STENT
| Applicant | Surgitek Medical Engineering Corp., Racine WI, US |
| Decision | Substantially Equivalent, Nov 19, 1991 |
| Received | Sep 3, 1991 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K913928
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.