510(k) K231709 ยท MQB Solid State X-Ray Imager (Flat Panel/Digital Imager)
AcuityDR 1013 G4, AcuityDR 1417 G4, AcuityDR 1717G4
| Applicant | Radmedix, LLC, Dayton OH, US |
| Decision | Substantially Equivalent, Jul 12, 2023 |
| Received | Jun 12, 2023 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K231709
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.