510(k) K905289 ยท FAD Stent, Ureteral
SURGITEK(R) LUBRI-FLEX(TM) URETERAL STENT
| Applicant | Medical Engineering Corp., Racine WI, US |
| Decision | Substantially Equivalent, Mar 13, 1991 |
| Received | Nov 26, 1990 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K905289
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.