Vascular Pathways, Inc. is one of 5098 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Vascular Pathways, Inc. - FDA 510(k) Cleared Devices
3
Total
3
Cleared
0
Denied
Vascular Pathways, Inc. has 3 FDA 510(k) cleared medical devices. Based in Orinda, US.
Historical record: 3 cleared submissions from 2011 to 2015. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Vascular Pathways, Inc. Filter by specialty or product code using the sidebar.
Vascular Pathways, Inc. — FDA 510(k) Products and Clearance History
3 devices
Cleared
Jan 08, 2015
ACCUCATH MIDLINE CATHETER SYSTEM
General Hospital
157d
Cleared
Jul 17, 2014
ACCUCATH BC INTRAVASCULAR CATHETER SYSTEM
General Hospital
140d
Cleared
Sep 22, 2011
RAPID INTRAVASCULAR CATHETER START SYSTEM 22 GAUGE / 20 GAUGE / 18 GAUGE
General Hospital
38d