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.
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.
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.


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