Vasocom, Inc. is one of 5134 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Vasocom, Inc. - FDA 510(k) Cleared Devices
3
Total
3
Cleared
0
Denied
Vasocom, Inc. has 3 FDA 510(k) cleared medical devices. Based in Bristol, US.
Historical record: 3 cleared submissions from 2008 to 2014. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Vasocom, Inc. Filter by specialty or product code using the sidebar.
Vasocom, Inc. — FDA 510(k) Products and Clearance History
3 devices
Cleared
Feb 12, 2014
PHYSIOFLOW Q-LINK
Cardiovascular
28d
Cleared
Dec 03, 2010
PHYSIOFLOW ENDURO
Cardiovascular
28d
Cleared
Apr 10, 2008
PHYSIOFLOW SYSTEM
Cardiovascular
786d