FDA 510(k) Applications Submitted by KONICA MINOLTA, INC.

FDA 510(k) Number	Submission Date	Device Name	Applicant
K250665	03/05/2025	SKR 3000	KONICA MINOLTA, INC.
K241319	05/10/2024	SKR 3000	Konica Minolta, Inc.
K141271	05/15/2014	AERODR SYSTEM 2	KONICA MINOLTA, INC.
K151060	04/20/2015	Ultrasound System SONIMAGE HS1	KONICA MINOLTA, INC.
K151465	06/01/2015	AeroDR SYSTEM 2	KONICA MINOLTA, INC.
K152577	09/09/2015	ULTRASOUND SYSTEM SONIMAGE HS 1	KONICA MINOLTA, INC.
K180084	01/11/2018	Ultrasound System SONIMAGE MX1	Konica Minolta, Inc.
K210066	01/11/2021	ImagePilot	Konica Minolta, Inc.
K240281	02/01/2024	Bone Suppression Software	Konica Minolta, Inc.
K210619	03/01/2021	SKR 3000	Konica Minolta, Inc.
K230906	03/31/2023	Konicaminolta DI-X1	Konica Minolta, Inc.
K220993	04/04/2022	Ultrasound System SONIMAGE MX1	Konica Minolta, INC.
K171716	06/09/2017	SKR 3000	Konica Minolta, Inc.
K191645	06/19/2019	SKR 4000	Konica Minolta, Inc.
K162065	07/26/2016	Ultrasound System SONIMAGE HS1	KONICA MINOLTA, INC.
K182153	08/08/2018	Ultrasound System SONIMAGE HS1	KONICA MINOLTA, INC.
K212685	08/24/2021	KONICAMINOLTA DI-X1	Konica Minolta, Inc.
K182431	09/06/2018	Konicaminolta DI-X1	Konica Minolta, Inc.
K172793	09/15/2017	SKR 3000	KONICA MINOLTA, INC.
K182688	09/26/2018	SKR 3000	KONICA MINOLTA, INC.
K223267	10/24/2022	SKR 3000	Konica Minolta, INC.
K213908	12/14/2021	SKR 3000	Konica Minolta, INC.