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FDA 510(k) Applications Submitted by Digimed Co., LTD.
FDA 510(k) Number
Submission Date
Device Name
Applicant
K220574
02/28/2022
HYBRID S70
Digimed Co., LTD.
K221587
06/01/2022
DHX-70H, XTG-70H
DIGIMED Co., Ltd.
K181891
07/13/2018
Portable X-ray System (Model: MiniX-V, Mini X-S)
Digimed Co., LTD.
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