Cpl Co., Ltd. is one of 449 FDA 510(k) medical device manufacturers from South Korea in the dataset, ranked by real submission volume.
Cpl Co., Ltd. - FDA 510(k) Cleared Devices
Recent clearances: CPL Insulin Pen Needle
1
Total
1
Cleared
0
Denied
Cpl Co., Ltd. has 1 FDA 510(k) cleared medical devices. Based in Ansan, KR.
Historical record: 1 cleared submissions from 2016 to 2016. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Cpl Co., Ltd. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Plusglobal as regulatory consultant.
FDA 510(k) Regulatory Record - Cpl Co., Ltd.
1 devices