Remedi Co., Ltd. - FDA 510(k) Cleared Devices
3
Total
3
Cleared
0
Denied
Remedi Co., Ltd. has 3 FDA 510(k) cleared medical devices. Based in Seoul, KR.
Latest FDA clearance: May 2024. Active since 2020. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Remedi Co., Ltd. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by 510K FDA, Inc. as regulatory consultant.
3 devices