R4 Vascular, Inc. is one of 5196 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
R4 Vascular, Inc. - FDA 510(k) Cleared Devices
7
Total
5
Cleared
0
Denied
R4 Vascular, Inc. has 5 FDA 510(k) cleared medical devices. Based in St. Paul, US.
Historical record: 5 cleared submissions from 2007 to 2013. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by R4 Vascular, Inc. Filter by specialty or product code using the sidebar.
R4 Vascular, Inc. — FDA 510(k) Products and Clearance History
7 devices
Cleared
Jun 06, 2013
VECTOR PTA BALLOON DILATATION CATHETER
Cardiovascular
29d
Cleared
Jun 14, 2012
VECTOR
Cardiovascular
37d
Cleared
Feb 18, 2010
DURASPAN HEMODIALYSIS LONG-TERM CATHETER
Gastroenterology & Urology
29d
Cleared
Jan 08, 2010
DURASPAN HEMODIALYSIS LONG-TERM CATHETER, MODELS 62152420, 621512820,...
Gastroenterology & Urology
232d
Cleared
Nov 18, 2009
PHEROCIOUS 10.5 FR (24 CM, 28 CM AND 32 CM), MODELS 430102440, 430102840,...
General Hospital
139d
Cleared
Mar 16, 2009
ZEUS CT PICC 4 FR AND 5 FR SINGLE AND DUAL LUMEN
General Hospital
88d
Cleared
Aug 20, 2007
R4 VASCULAR INC. PEGASUS CT PICC, MODEL 500005-001,002, 004, 005, 500004-001,...
General Hospital
97d