Vascumetrix, LLC is one of 25854 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Vascumetrix, LLC - FDA 510(k) Cleared Devices
Recent clearances: GELBFISH FLEX VASCULAR DILATOR, MODIFICATION TO GELBFISH VASCULAR DILATORS, GELBISH VASCULAR DILATOR
3
Total
3
Cleared
0
Denied
Vascumetrix, LLC has 3 FDA 510(k) cleared medical devices. Based in Meas, US.
Historical record: 3 cleared submissions from 2001 to 2003. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Vascumetrix, LLC Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Vascumetrix, LLC
3 devices