Vector Corporation, LLC is one of 19562 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Vector Corporation, LLC - FDA 510(k) Cleared Devices
Recent clearances: Vector PTA Balloon Dilatation Catheter
1
Total
1
Cleared
0
Denied
Vector Corporation, LLC has 1 FDA 510(k) cleared medical devices. Based in New York, US.
Historical record: 1 cleared submissions from 2015 to 2015. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Vector Corporation, LLC Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Honkanen Consulting, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Vector Corporation, LLC
1 devices