FDA 510(k) Applications Submitted by Tsutomu Fukui
FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
K180084 |
01/11/2018 |
Ultrasound System SONIMAGE MX1 |
Konica Minolta, Inc. |
K210066 |
01/11/2021 |
ImagePilot |
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. |
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