Cardiosolutions, Inc. is one of 5135 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Cardiosolutions, Inc. - FDA 510(k) Cleared Devices
4
Total
4
Cleared
0
Denied
Cardiosolutions, Inc. has 4 FDA 510(k) cleared medical devices. Based in Stoughton, US.
Historical record: 4 cleared submissions from 2010 to 2014. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Cardiosolutions, Inc. Filter by specialty or product code using the sidebar.
Cardiosolutions, Inc. — FDA 510(k) Products and Clearance History
4 devices
Cleared
Feb 05, 2014
CARDIOSOLUTIONS DEXTERITY STEERABLE INTRODUCER
Cardiovascular
34d
Cleared
Jul 19, 2013
CARDIOSOLUTIONS PERCU-PRO STEERABLE INTRODUCER
Cardiovascular
71d
Cleared
Jul 14, 2011
PERCUPRO MESSENGER BALLOON CATHETER
Cardiovascular
560d
Cleared
Sep 27, 2010
PERCU-PRO GUIDEWIRE
Cardiovascular
270d