FDA 510(k) Applications Submitted by Finemedix Co., Ltd.

FDA 510(k) Number Submission Date Device Name Applicant
K200217 01/28/2020 ClearEndoclip Finemedix Co., Ltd.
K183289 11/26/2018 ClearGrasp Snare Finemedix Co., Ltd.
K183021 11/01/2018 ClearEndoclip Finemedix Co., Ltd.
K231267 05/02/2023 ClearTip Finemedix Co., Ltd.
K202616 09/09/2020 ClearCap Distal Attachment Finemedix Co., Ltd.


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