FDA 510(k) Applications Submitted by CIMILRE CO., LTD.

FDA 510(k) Number Submission Date Device Name Applicant
K162870 10/13/2016 CIMLRE F1 and CIMILRE S3 CIMILRE CO., LTD.
K221708 06/13/2022 CIMILRE Free-T2 Plus Cimilre Co., Ltd.


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