510(k) K102408 ยท KPR System, X-Ray, Stationary
DIGITAL DIAGNOSTIC X-RAY SYSTEM
| Applicant | DRGEM Corporation, Echo OR, US |
| Decision | Substantially Equivalent, Dec 27, 2010 |
| Received | Aug 23, 2010 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K102408
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.