Bc Group International, Inc. is one of 18943 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Bc Group International, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Defibrillator Analyzer Variable Load, DEFIBRILLATOR ANALYZER - DA-2006P
2
Total
2
Cleared
0
Denied
Bc Group International, Inc. has 2 FDA 510(k) cleared medical devices. Based in Oak Grove, US.
Historical record: 2 cleared submissions from 2011 to 2015. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Bc Group International, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Intertek Testing Services as regulatory consultant.
FDA 510(k) Regulatory Record - Bc Group International, Inc.
2 devices