Konica Minolta Medical & Graphic, Inc. is one of 79 FDA 510(k) medical device manufacturers from Japan in the dataset, ranked by real submission volume.
Konica Minolta Medical & Graphic, Inc. - FDA 510(k) Cleared Devices
Recent clearances: AERODR SYSTEM WITH P-31, AEROPILOT, AERODR STITCHING SYSTEM
27
Total
27
Cleared
0
Denied
Konica Minolta Medical & Graphic, Inc. has 27 FDA 510(k) cleared radiology devices. Based in Hachioji-Shi Tokyo, JP.
Historical record: 27 cleared submissions from 2002 to 2013.
Browse the complete list of FDA 510(k) cleared radiology devices from this manufacturer. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Intertek Testing Services as regulatory consultant.
FDA 510(k) Regulatory Record - Konica Minolta Medical & Graphic, Inc.
27 devices
Cleared
Aug 22, 2013
AERODR SYSTEM WITH P-31
Radiology
140d
Cleared
Dec 20, 2012
AEROPILOT
Radiology
37d
Cleared
Jun 08, 2012
AERODR STITCHING SYSTEM
Radiology
88d
Cleared
May 23, 2012
AERODR X70
Radiology
41d
Cleared
Apr 09, 2012
AEROSYNC FOR AERODR SYSTEM
Radiology
53d
Cleared
Feb 10, 2012
REGIUS SIGMA2
Radiology
24d
Cleared
Jan 17, 2012
AERODR SYSTEM WITH P-21
Radiology
75d
Cleared
Dec 23, 2011
KONICA MINOLTA XPRESS DIGITAL MAMMOGRAPHY SYSTEM
Radiology
283d
Cleared
Jun 02, 2011
REGUIS SIGMA
Radiology
164d
Cleared
Feb 04, 2011
ACIES
Radiology
218d
Cleared
Nov 24, 2010
AERODR SYSTEM
Radiology
97d
Cleared
Oct 30, 2009
DIRECT DIGITIZER, REGIUS MODEL 210
Radiology
57d