Mico Biomed Co., Ltd. is one of 419 FDA 510(k) medical device manufacturers from South Korea in the dataset, ranked by real submission volume.
Mico Biomed Co., Ltd. - FDA 510(k) Cleared Devices
Recent clearances: VERI-Q MGD-1001 BLOOD GLUCOSE MONITORING SYSTEM, VERI-Q PLUS MGD-1001 BLOOD GLUCOSE MONITORING SYSTEM, VERI-Q SELF-TESTING AND VERI-Q PLUS MGD-2001 BLOOD GLUCOSE MONITORING SYSTEMS
2
Total
2
Cleared
0
Denied
Mico Biomed Co., Ltd. has 2 FDA 510(k) cleared medical devices. Based in Anseong, KR.
Historical record: 2 cleared submissions from 2013 to 2013. Primary specialty: Chemistry.
Browse the FDA 510(k) cleared devices submitted by Mico Biomed Co., Ltd. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Mico Biomed Co., Ltd.
2 devices