ClearanceBrief
510(k) K042133 ยท LMC Camera, Multi Format, Radiological

DRY LASER IMAGER, MODEL DRYPRO MODEL 793

ApplicantKonica Minolta Medical & Graphic, Inc., Watarai-Gun; Mie-Ken, JP
DecisionSubstantially Equivalent, Nov 24, 2004
ReceivedAug 9, 2004
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K042133

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.