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Konica Minolta Medical & Graphic, Inc.

FDA 510(k) & PMA Approved Devices — 27 products

Total Devices27
Categories0
Latest FDA decision
TypeNumberDevice NameCodeDateActions
510(k) K130936 AERODR SYSTEM WITH P-31MQB2013-08-22 View
510(k) K123499 AEROPILOTMQB2012-12-20 View
510(k) K120752 AERODR STITCHING SYSTEMKPR2012-06-08 View
510(k) K121109 AERODR X70KPR2012-05-23 View
510(k) K120477 AEROSYNC FOR AERODR SYSTEMMQB2012-04-09 View
510(k) K120131 REGIUS SIGMA2MQB2012-02-10 View
510(k) K113248 AERODR SYSTEM WITH P-21KPR2012-01-17 View
510(k) K110717 KONICA MINOLTA XPRESS DIGITAL MAMMOGRAPHY SYSTEMMUE2011-12-23 View
510(k) K103703 REGUIS SIGMAMQB2011-06-02 View
510(k) K101842 ACIESLLZ2011-02-04 View
510(k) K102349 AERODR SYSTEMKPR2010-11-24 View
510(k) K092717 DIRECT DIGITIZER, REGIUS MODEL 210MQB2009-10-30 View
510(k) K081637 LASER IMAGER DRYPRO MODEL 873LMC2008-07-01 View
510(k) K071436 REGIUS UNITEALLZ2007-06-27 View
510(k) K071181 DIRECT DIGITIZER, REGIUS MODEL 110MQB2007-05-30 View
510(k) K061999 DRY LASER IMAGER, DRYPRO MODEL 832LMC2006-08-15 View
510(k) K053173 DS CASSETTEIXA2005-12-15 View
510(k) K052095 MODIFICATION TO: DIRECT DIGITIZER REGIUS MODEL 190MQB2005-11-03 View
510(k) K051998 REGIUS MODEL 170 DIRECT DIGITIZERMQB2005-11-03 View
510(k) K051523 REGIUS CONSOLE CS-2000 AND REGIUS CONSOLE CS-3000, MEDICAL IMAGE PROCESSING WORKSTATIONLLZ2005-07-20 View
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