510(k) K061548 ยท FCS Light, Catheter, Fiberoptic, Glass, Ureteral
STRYKER URETERAL ILLUMINATION SYSTEM IV
| Applicant | Stryker Corp., San Jose CA, US |
| Decision | Substantially Equivalent, Sep 28, 2006 |
| Received | Jun 5, 2006 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K061548
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.