510(k) K092830 ยท KPR System, X-Ray, Stationary
DIGITAL X-RAY IMAGING SYSTEM, MODEL DRC-1000
| Applicant | VATECH Co., Ltd., Houston TX, US |
| Decision | Substantially Equivalent, Jul 21, 2010 |
| Received | Sep 14, 2009 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K092830
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.