FDA 510(k) Applications Submitted by RUSSEL MUNVES
| FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
| K120752 |
03/12/2012 |
AERODR STITCHING SYSTEM |
KONICA MINOLTA MEDICAL & GRAPHIC, INC. |
| K130936 |
04/04/2013 |
AERODR SYSTEM WITH P-31 |
KONICA MINOLTA MEDICAL & GRAPHIC, INC. |
| K071181 |
04/30/2007 |
DIRECT DIGITIZER, REGIUS MODEL 110 |
KONICA MINOLTA MEDICAL & GRAPHIC, INC. |
| K082347 |
08/15/2008 |
DIGITAL RADIOGRAPHY, FLEXDR C30 |
KONICA MINOLTA TECHNOPRODUCT CO., LTD. |
| K092717 |
09/03/2009 |
DIRECT DIGITIZER, REGIUS MODEL 210 |
KONICA MINOLTA MEDICAL & GRAPHIC, INC. |
| K120131 |
01/17/2012 |
REGIUS SIGMA2 |
KONICA MINOLTA MEDICAL & GRAPHIC, INC. |
| K071436 |
05/23/2007 |
REGIUS UNITEA |
KONICA MINOLTA MEDICAL & GRAPHIC, INC. |
| K081637 |
06/11/2008 |
LASER IMAGER DRYPRO MODEL 873 |
KONICA MINOLTA MEDICAL & GRAPHIC, INC. |
| K101842 |
07/01/2010 |
ACIES |
KONICA MINOLTA MEDICAL & GRAPHIC, INC. |
| K102349 |
08/19/2010 |
AERODR SYSTEM |
KONICA MINOLTA MEDICAL & GRAPHIC, INC. |
| K113248 |
11/03/2011 |
AERODR SYSTEM WITH P-21 |
KONICA MINOLTA MEDICAL & GRAPHIC, INC. |
| K123499 |
11/13/2012 |
AEROPILOT |
KONICA MINOLTA MEDICAL & GRAPHIC, INC. |
| K133730 |
12/06/2013 |
CO PILOT/REGIUS UNITEA |
KONICA MINOLTA INC. |
| K103703 |
12/20/2010 |
REGUIS SIGMA |
KONICA MINOLTA MEDICAL & GRAPHIC, INC. |
| K990359 |
02/05/1999 |
KONICA DIRECT DIGITIZER, MODEL DD-341 |
KONICA CORP. |
| K980873 |
03/06/1998 |
KONICA DIRECT DIGITIZER REGIUS MODEL 330 |
KONICA CORP. |
| K990969 |
03/23/1999 |
KONICA SRX- 701 AUTOMATIC X-RAY FILM PROCESSOR |
KONICA MEDICAL CORP. |
| K141271 |
05/15/2014 |
AERODR SYSTEM 2 |
KONICA MINOLTA, INC. |
| K963913 |
09/30/1996 |
MD100 & MM150 |
KONICA MEDICAL CORP. |
| K963914 |
09/30/1996 |
CM & CM DS-7 |
KONICA MEDICAL CORP. |
| K955583 |
12/05/1995 |
VIFS |
KONICA MEDICAL CORP. |
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