Medical Device Manufacturer · KR , Paju-Si

Sejong Medical Co., Ltd. - FDA 510(k) Cleared Devices

7 submissions · 7 cleared · Since 2017
7
Total
7
Cleared
0
Denied

Sejong Medical Co., Ltd. has 7 FDA 510(k) cleared medical devices. Based in Paju-Si, KR.

Last cleared in 2021. Active since 2017. Primary specialty: General & Plastic Surgery.

Browse the FDA 510(k) cleared devices submitted by Sejong Medical Co., Ltd. Filter by specialty or product code using the sidebar.

510(k) submissions have been managed by LK Consulting Group USA, Inc. as regulatory consultant.

FDA 510(k) Regulatory Record - Sejong Medical Co., Ltd.
7 devices
1-7 of 7
Filters