Intervascular is one of 24547 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Intervascular - FDA 510(k) Cleared Devices
Recent clearances: INTERGARD WOVEN CONNECTOR GRAFT, MODEL IGW0030-10C, INTERVASCULAR INTERGARD KNITTED VASCULAR GRAFT SIZER, INTERGARD HEMABRIDGE COLLAGEN COATED VASCULAR PROSTHESIS, INTERGARD AORTIC ARCH COLLAGEN COATED VASCULAR PROSTHESIS
3
Total
3
Cleared
0
Denied
Intervascular has 3 FDA 510(k) cleared medical devices. Based in Wellesley, US.
Historical record: 3 cleared submissions from 2002 to 2005. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Intervascular Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Intervascular
3 devices
Cleared
Feb 18, 2005
INTERGARD WOVEN CONNECTOR GRAFT, MODEL IGW0030-10C
Cardiovascular
112d
Cleared
Aug 14, 2002
INTERVASCULAR INTERGARD KNITTED VASCULAR GRAFT SIZER
Cardiovascular
34d
Cleared
Feb 27, 2002
INTERGARD HEMABRIDGE COLLAGEN COATED VASCULAR PROSTHESIS, INTERGARD AORTIC...
Cardiovascular
113d