510(k) K942688 ยท LJE Catheter, Nephrostomy
NEPHRO-URETERAL STENT
| Applicant | Uresil Corp., Skokie IL, US |
| Decision | Substantially Equivalent, Jun 6, 1995 |
| Received | Jun 7, 1994 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K942688
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.