Wettrust Korea Co., Ltd. is one of 419 FDA 510(k) medical device manufacturers from South Korea in the dataset, ranked by real submission volume.
Wettrust Korea Co., Ltd. - FDA 510(k) Cleared Devices
Recent clearances: wettrust D2care
1
Total
1
Cleared
0
Denied
Wettrust Korea Co., Ltd. has 1 FDA 510(k) cleared medical devices. Based in Seongnam, KR.
Historical record: 1 cleared submissions from 2017 to 2017. Primary specialty: Obstetrics & Gynecology.
Browse the FDA 510(k) cleared devices submitted by Wettrust Korea Co., Ltd. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Mdi Consultant, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Wettrust Korea Co., Ltd.
1 devices