510(k) K131226 ยท FCW Light Source, Fiberoptic, Routine
NOVAPROBE LED LIGHT SOURCE
| Applicant | Novaprobe Incorporated, Lansdale PA, US |
| Decision | Substantially Equivalent, Jul 24, 2014 |
| Received | Apr 30, 2013 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K131226
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.