FDA 510(k) Applications Submitted by Nariaki Morita

FDA 510(k) Number Submission Date Device Name Applicant
K190573 03/06/2019 KOWA DR-1a Kowa Company, Ltd.
K191945 07/22/2019 KOWA nonmyd 8 Kowa Company, Ltd.
K222372 08/05/2022 Kowa SL-19 Kowa Company, Ltd.


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