510(k) K121724 ยท FCW Light Source, Fiberoptic, Routine
ENDOLIGHT LED 1.1 ENDOLIGHTLED 1.2
| Applicant | Richard Wolf Medical Instruments Corp., Vernon Hills IL, US |
| Decision | Substantially Equivalent, Sep 20, 2012 |
| Received | Jun 12, 2012 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K121724
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.