510(k) K980889 ยท LJE Catheter, Nephrostomy
URESIL NEPHRO-URETERAL STENT
| Applicant | Uresil Corp., Skokie IL, US |
| Decision | Substantially Equivalent, Apr 8, 1998 |
| Received | Mar 9, 1998 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K980889
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.