Imani Co. - FDA 510(k) Cleared Devices
3
Total
3
Cleared
0
Denied
Imani Co. has 3 FDA 510(k) cleared medical devices. Based in Yongin-Si, KR.
Last cleared in 2023. Active since 2021. Primary specialty: Obstetrics & Gynecology.
Browse the FDA 510(k) cleared devices submitted by Imani Co. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Global Medical Standard Consulting Co., Ltd. as regulatory consultant.
FDA 510(k) Regulatory Record - Imani Co.
3 devices