510(k) K131434 ยท GWG Endoscope, Neurological
VS3 STEREOSCOPIC HIGH DEFINITION VISION SYSTEM
| Applicant | Visionsense, Ltd., Washington DC, US |
| Decision | Substantially Equivalent, Jul 16, 2013 |
| Received | May 17, 2013 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K131434
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.