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Konica Minolta, Inc.

FDA 510(k) & PMA Approved Devices — 19 products

Total Devices19
Categories4
Latest Approval2025-06-17
TypeNumberDevice NameCodeDate
510(k) K250665 SKR 3000 MQB 2025-06-17 View
510(k) K241319 SKR 3000 MQB 2024-11-21 View
510(k) K240281 Bone Suppression Software LLZ 2024-05-31 View
510(k) K230906 Konicaminolta DI-X1 LLZ 2023-04-25 View
510(k) K223267 SKR 3000 MQB 2022-11-17 View
510(k) K220993 Ultrasound System SONIMAGE MX1 IYN 2022-06-23 View
510(k) K213908 SKR 3000 MQB 2022-01-31 View
510(k) K212685 KONICAMINOLTA DI-X1 LLZ 2021-09-13 View
510(k) K210619 SKR 3000 MQB 2021-08-24 View
510(k) K210066 ImagePilot LLZ 2021-05-06 View
510(k) K191645 SKR 4000 MQB 2019-08-16 View
510(k) K182688 SKR 3000 MQB 2018-12-18 View
510(k) K182431 Konicaminolta DI-X1 LLZ 2018-11-26 View
510(k) K182153 Ultrasound System SONIMAGE HS1 IYO 2018-09-06 View
510(k) K180084 Ultrasound System SONIMAGE MX1 IYO 2018-02-08 View
510(k) K172793 SKR 3000 MQB 2017-10-12 View
510(k) K171716 SKR 3000 MQB 2017-08-25 View
510(k) K162065 Ultrasound System SONIMAGE HS1 IYN 2016-10-19 View
510(k) K162504 SKR 3000 MQB 2016-10-03 View
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