510(k) K092717 ยท MQB Solid State X-Ray Imager (Flat Panel/Digital Imager)
DIRECT DIGITIZER, REGIUS MODEL 210
| Applicant | Konica Minolta Medical & Graphic, Inc., New York NY, US |
| Decision | Substantially Equivalent, Oct 30, 2009 |
| Received | Sep 3, 2009 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K092717
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.