ClearanceBrief
510(k) K023061 ยท MQB Solid State X-Ray Imager (Flat Panel/Digital Imager)

KONICA DIRECT DIGITIZER REGIUS, MODEL 170

ApplicantKonica Minolta Medical & Graphic, Inc., Hachioji-Shi Tokyo, JP
DecisionSubstantially Equivalent, Oct 11, 2002
ReceivedSep 16, 2002
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K023061

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.