Cardio-Vascular Innovations, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Cardio-Vascular Innovations, Inc. - FDA 510(k) Cleared Devices
4
Total
4
Cleared
0
Denied
Cardio-Vascular Innovations, Inc. has 4 FDA 510(k) cleared medical devices. Based in Chantilly, US.
Historical record: 4 cleared submissions from 1984 to 1987. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Cardio-Vascular Innovations, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Cardio-Vascular Innovations, Inc.
4 devices
Cleared
Jan 06, 1987
CVI 16 GAUGE CENTRAL VEIN CATHERIZATION SYSTEM
Cardiovascular
90d
Cleared
Jan 06, 1987
CVI 8.5 FRENCH PERCUTANEOUS SHEATH INTRODUCER SYS.
Cardiovascular
90d
Cleared
Nov 05, 1985
7 FRENCH DUAL LUMEN COM CENT VEIN CATH SYS
Cardiovascular
127d
Cleared
Oct 18, 1984
FRENCH 7 TRI-ACCESS COMPACT CENTRAL VEIN
Cardiovascular
42d