Company ยท US
Konica Minolta Medical & Graphic, Inc.
FDA 510(k) clearances and medical device recalls filed under this name, 2002 to 2013. Name variants (Inc, Corp, punctuation) are merged.
27510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)
Product codes
Latest 510(k) clearances
| Decided | 510(k) | Device and applicant | Code |
|---|---|---|---|
| Aug 22, 2013 | K130936 | AERODR SYSTEM WITH P-31 Konica Minolta Medical & Graphic, Inc. | MQB |
| Dec 20, 2012 | K123499 | AEROPILOT Konica Minolta Medical & Graphic, Inc. | MQB |
| Jun 8, 2012 | K120752 | AERODR STITCHING SYSTEM Konica Minolta Medical & Graphic, Inc. | KPR |
| May 23, 2012 | K121109 | AERODR X70 Konica Minolta Medical & Graphic, Inc., JP | KPR |
| Apr 9, 2012 | K120477 | AEROSYNC FOR AERODR SYSTEM Konica Minolta Medical & Graphic, Inc. | MQB |
| Feb 10, 2012 | K120131 | REGIUS SIGMA2 Konica Minolta Medical & Graphic, Inc. | MQB |
| Jan 17, 2012 | K113248 | AERODR SYSTEM WITH P-21 Konica Minolta Medical & Graphic, Inc. | KPR |
| Dec 23, 2011 | K110717 | KONICA MINOLTA XPRESS DIGITAL MAMMOGRAPHY SYSTEM Konica Minolta Medical & Graphic, Inc. | MUE |
| Jun 2, 2011 | K103703 | REGUIS SIGMA Konica Minolta Medical & Graphic, Inc. | MQB |
| Feb 4, 2011 | K101842 | ACIES Konica Minolta Medical & Graphic, Inc. | LLZ |
| Nov 24, 2010 | K102349 | AERODR SYSTEM Konica Minolta Medical & Graphic, Inc. | KPR |
| Oct 30, 2009 | K092717 | DIRECT DIGITIZER, REGIUS MODEL 210 Konica Minolta Medical & Graphic, Inc. | MQB |
| Jul 1, 2008 | K081637 | LASER IMAGER DRYPRO MODEL 873 Konica Minolta Medical & Graphic, Inc. | LMC |
| Jun 27, 2007 | K071436 | REGIUS UNITEA Konica Minolta Medical & Graphic, Inc. | LLZ |
| May 30, 2007 | K071181 | DIRECT DIGITIZER, REGIUS MODEL 110 Konica Minolta Medical & Graphic, Inc. | MQB |
| Aug 15, 2006 | K061999 | DRY LASER IMAGER, DRYPRO MODEL 832 Konica Minolta Medical & Graphic, Inc., JP | LMC |
| Dec 15, 2005 | K053173 | DS CASSETTE Konica Minolta Medical & Graphic, Inc., JP | IXA |
| Nov 3, 2005 | K052095 | MODIFICATION TO: DIRECT DIGITIZER REGIUS MODEL 190 Konica Minolta Medical & Graphic, Inc., JP | MQB |
| Nov 3, 2005 | K051998 | REGIUS MODEL 170 DIRECT DIGITIZER Konica Minolta Medical & Graphic, Inc., JP | MQB |
| Jul 20, 2005 | K051523 | REGIUS CONSOLE CS-2000 AND REGIUS CONSOLE CS-3000, MEDICAL IMAGE PROCESSING WORKSTATION Konica Minolta Medical & Graphic, Inc., JP | LLZ |
| Jul 1, 2005 | K051418 | DIRECT DIGITIZER REGIUS MODEL 370 Konica Minolta Medical & Graphic, Inc., JP | MQB |
| Jun 28, 2005 | K051521 | REGIUS RS-1000, MEDICAL IMAGE PROCESSING WORKSTATION Konica Minolta Medical & Graphic, Inc., JP | LLZ |
| Dec 15, 2004 | K042386 | DIRECT DIGITIZER, REGIUS MODEL 190 Konica Minolta Medical & Graphic, Inc., JP | MQB |
| Nov 24, 2004 | K042133 | DRY LASER IMAGER, MODEL DRYPRO MODEL 793 Konica Minolta Medical & Graphic, Inc., JP | LMC |
| Oct 11, 2002 | K023061 | KONICA DIRECT DIGITIZER REGIUS, MODEL 170 Konica Minolta Medical & Graphic, Inc., JP | MQB |
| Mar 1, 2002 | K013054 | KONICA DIRECT DIGITIZER REGIUS MODEL 350 Konica Minolta Medical & Graphic, Inc., JP | MQB |
| Jan 16, 2002 | K013052 | KONICA LASER IMAGER, DRYPRO MODEL 751/752 Konica Minolta Medical & Graphic, Inc., JP | LMC |
Latest recalls
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| No recalls in this window. | |||