Medical Device Manufacturer · US , New York , NY

Konica Minolta, Inc. - FDA 510(k) Cleared Devices

25 submissions · 25 cleared · Since 2014

Recent clearances: SKR 3000, SKR 3000, Bone Suppression Software

Official Website
25
Total
25
Cleared
0
Denied

FDA 510(k) Regulatory Record - Konica Minolta, Inc. Radiology ✕

25 devices
1-12 of 25
Cleared Jun 17, 2025
SKR 3000
K250665 · MQB
Radiology · 104d
Cleared Nov 21, 2024
SKR 3000
K241319 · MQB
Radiology · 195d
Cleared May 31, 2024
Bone Suppression Software
K240281 · LLZ
Radiology · 120d
Cleared Apr 25, 2023
Konicaminolta DI-X1
K230906 · LLZ
Radiology · 25d
Cleared Nov 17, 2022
SKR 3000
K223267 · MQB
Radiology · 24d
Cleared Jun 23, 2022
Ultrasound System SONIMAGE MX1
K220993 · IYN
Radiology · 80d
Cleared Jan 31, 2022
SKR 3000
K213908 · MQB
Radiology · 48d
Cleared Sep 13, 2021
KONICAMINOLTA DI-X1
K212685 · LLZ
Radiology · 20d
Cleared Aug 24, 2021
SKR 3000
K210619 · MQB
Radiology · 176d
Cleared May 06, 2021
ImagePilot
K210066 · LLZ
Radiology · 115d
Cleared Aug 16, 2019
SKR 4000
K191645 · MQB
Radiology · 58d
Cleared Dec 18, 2018
SKR 3000
K182688 · MQB
Radiology · 83d
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