FDA 510(k) Applications Submitted by Dong Hoon Shin

FDA 510(k) Number Submission Date Device Name Applicant
K203142 10/20/2020 Veuron-Brain-pAb Heuron Co., Ltd.
K203279 11/06/2020 Veuron-Brain-mN1 Heuron Co., Ltd.
K213801 12/06/2021 Veuron-Brain-pAb2 Heuron Co., Ltd.
K201776 06/29/2020 Foley Balloon Catheter for Urology Apollon co., Ltd.
K193031 10/30/2019 EXPD 4343P, EXPD 3643P DRTECH Corporation


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