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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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