510(k) K982542 ยท FCS Light, Catheter, Fiberoptic, Glass, Ureteral
STRYKER URETERAL ILLUMINATOR SYSTEM III
| Applicant | Stryker Endoscopy, Santa Clara CA, US |
| Decision | Substantially Equivalent, Sep 22, 1998 |
| Received | Jul 21, 1998 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K982542
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Sep 16, 2008 | Stryker Endoscopy Stryker Ureteral Kit, Model number 220-180-516, The ureteral kit is a ureteral transillumination device with reusable illumination source and a fiberoptic light ureteral catheter kit which is provided Terminated |
FCS | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.