ClearanceBrief
510(k) K051418 ยท MQB Solid State X-Ray Imager (Flat Panel/Digital Imager)

DIRECT DIGITIZER REGIUS MODEL 370

ApplicantKonica Minolta Medical & Graphic, Inc., Mie-Ken, JP
DecisionSubstantially Equivalent, Jul 1, 2005
ReceivedJun 1, 2005
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K051418

DateFirm and productCodeLinked 510(k)
Aug 31, 2006Konica Minolta Medical Imaging USA, Inc.
Regius Model 370 Digital Radiography Konica Minolta
Terminated
MQBNone listed

Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.