Vasonova, Inc. is one of 19105 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Vasonova, Inc. - FDA 510(k) Cleared Devices
Recent clearances: VASCULAR POSITIONING SYSTEM (VPS) G4 CONSOLE, VASCULAR POSITIONING SYSTEM TM (VPS TM SYSTEM) STYLET, VASCULAR POSITIONING SYSTEM (VPS SYSTEM) CONSOLE
8
Total
8
Cleared
0
Denied
Vasonova, Inc. has 8 FDA 510(k) cleared medical devices. Based in Sunnyvale, US.
Historical record: 8 cleared submissions from 2008 to 2013. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Vasonova, Inc. Filter by specialty or product code using the sidebar.
2 devices have linked clinical trials registered on ClinicalTrials.gov.
FDA 510(k) Regulatory Record - Vasonova, Inc.
8 devices
Cleared
Jan 18, 2013
VASCULAR POSITIONING SYSTEM (VPS) G4 CONSOLE
Cardiovascular
38d
Cleared
CT
Feb 18, 2011
VASCULAR POSITIONING SYSTEM TM (VPS TM SYSTEM) STYLET
Cardiovascular
107d
Cleared
CT
Feb 18, 2011
VASCULAR POSITIONING SYSTEM (VPS SYSTEM) CONSOLE
Cardiovascular
106d
Cleared
Nov 18, 2009
VPS CATHETER
General Hospital
141d
Cleared
May 01, 2009
FLOWPICC CATHETER
General Hospital
121d
Cleared
Dec 17, 2008
FLOWPICC CATHETER
General Hospital
111d
Cleared
Oct 15, 2008
FLOWPICC CONSOLE
Cardiovascular
127d
Cleared
Sep 26, 2008
FLOWPICC STYLET
Cardiovascular
108d