Konica Minolta, Inc. - FDA 510(k) Cleared Devices
25
Total
25
Cleared
0
Denied
FDA 510(k) cleared devices by Konica Minolta, Inc. Radiology ✕
25 devices
Cleared
Jun 17, 2025
SKR 3000
Radiology
104d
Cleared
Nov 21, 2024
SKR 3000
Radiology
195d
Cleared
May 31, 2024
Bone Suppression Software
Radiology
120d
Cleared
Apr 25, 2023
Konicaminolta DI-X1
Radiology
25d
Cleared
Nov 17, 2022
SKR 3000
Radiology
24d
Cleared
Jun 23, 2022
Ultrasound System SONIMAGE MX1
Radiology
80d
Cleared
Jan 31, 2022
SKR 3000
Radiology
48d
Cleared
Sep 13, 2021
KONICAMINOLTA DI-X1
Radiology
20d
Cleared
Aug 24, 2021
SKR 3000
Radiology
176d
Cleared
May 06, 2021
ImagePilot
Radiology
115d
Cleared
Aug 16, 2019
SKR 4000
Radiology
58d
Cleared
Dec 18, 2018
SKR 3000
Radiology
83d
Cleared
Nov 26, 2018
Konicaminolta DI-X1
Radiology
81d
Cleared
Sep 06, 2018
Ultrasound System SONIMAGE HS1
Radiology
29d
Cleared
Feb 08, 2018
Ultrasound System SONIMAGE MX1
Radiology
28d
Cleared
Oct 12, 2017
SKR 3000
Radiology
27d
Cleared
Aug 25, 2017
SKR 3000
Radiology
77d
Cleared
Oct 19, 2016
Ultrasound System SONIMAGE HS1
Radiology
85d
Cleared
Oct 03, 2016
SKR 3000
Radiology
26d
Cleared
Oct 08, 2015
ULTRASOUND SYSTEM SONIMAGE HS 1
Radiology
29d
Cleared
Jun 29, 2015
AeroDR SYSTEM 2
Radiology
28d
Cleared
Jun 05, 2015
Ultrasound System SONIMAGE HS1
Radiology
46d
Cleared
Nov 21, 2014
ULTRASOUND SYSTEM SONIMAGE HS1, LINEAR PROBE L18-4, CONVEX PROBE C5-2
Radiology
102d
Cleared
Sep 26, 2014
AERODR SYSTEM 2
Radiology
134d
Cleared
Jan 31, 2014
CO PILOT/REGIUS UNITEA
Radiology
56d