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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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