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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