Chungwoo Co., Ltd. - FDA 510(k) Cleared Devices
2
Total
2
Cleared
0
Denied
Chungwoo Co., Ltd. has 2 FDA 510(k) cleared medical devices. Based in Seoul, KR.
Latest FDA clearance: May 2024. Active since 2023. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Chungwoo Co., Ltd. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by KMC, Inc. as regulatory consultant.
2 devices