FDA 510(k) Applications Submitted by YOUNGBAE KWON

FDA 510(k) Number Submission Date Device Name Applicant
K220579 02/21/2022 Hybrid C70 Digimed Co., Ltd
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.
K152859 09/30/2015 Portable X-ray System (Model: MINIX-V / MINIX-S) DIGIMED CO., LTD. (DIGIMED CORPORATION UNTIL 31/12/2012)


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