Hosuk Co., Ltd. is one of 468 FDA 510(k) medical device manufacturers from South Korea in the dataset, ranked by real submission volume.
Hosuk Co., Ltd. - FDA 510(k) Cleared Devices
Recent clearances: SUREONE INSULIN SYRINGE, 31 GAUGE X 5/16, SUREONE INSULIN SYRINGE
2
Total
2
Cleared
0
Denied
Hosuk Co., Ltd. has 2 FDA 510(k) cleared medical devices. Based in Umsung-Gun, Chungcheong, KR.
Historical record: 2 cleared submissions from 2000 to 2002. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Hosuk Co., Ltd. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Tuv Product Service, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Hosuk Co., Ltd.
2 devices