510(k) K123106 ยท KPR System, X-Ray, Stationary
DIGITAL DIAGNOSTIC X-RAY SYSTEM MODEL XGEO GU60A
| Applicant | Samsung Electronics Co., Ltd., Echo OR, US |
| Decision | Substantially Equivalent, Jun 20, 2013 |
| Received | Oct 2, 2012 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K123106
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.