Sang-A Frontec Co., Ltd. is one of 351 FDA 510(k) medical device manufacturers from South Korea in the dataset, ranked by real submission volume.
Sang-A Frontec Co., Ltd. - FDA 510(k) Cleared Devices
Recent clearances: Greenmedi Safety Filter Syringe
1
Total
1
Cleared
0
Denied
Sang-A Frontec Co., Ltd. has 1 FDA 510(k) cleared medical devices. Based in Incheon, KR.
Historical record: 1 cleared submissions from 2019 to 2019. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Sang-A Frontec 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 - Sang-A Frontec Co., Ltd.
1 devices