ClearanceBrief
510(k) K061999 ยท LMC Camera, Multi Format, Radiological

DRY LASER IMAGER, DRYPRO MODEL 832

ApplicantKonica Minolta Medical & Graphic, Inc., Hachioji-Shi, JP
DecisionSubstantially Equivalent, Aug 15, 2006
ReceivedJul 14, 2006
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K061999

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.