FDA 510(k) Applications Submitted by Remedi Co. Ltd.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K200284 | 02/05/2020 | R-Sensor, R-Sensor | Remedi Co. Ltd. |
| K212144 | 07/09/2021 | Remex KA6 | Remedi Co. Ltd. |
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