Cryo Vascular Systems, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Cryo Vascular Systems, Inc. - FDA 510(k) Cleared Devices
7
Total
7
Cleared
0
Denied
Cryo Vascular Systems, Inc. has 7 FDA 510(k) cleared medical devices. Based in Lost Gatos, US.
Historical record: 7 cleared submissions from 2002 to 2005. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Cryo Vascular Systems, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Cryo Vascular Systems, Inc.
7 devices
Cleared
Aug 05, 2005
POLAR CATH PERIPHERAL DILATATION SYSTEM
Cardiovascular
21d
Cleared
Nov 05, 2004
POLARCATH PERIPHERAL BALLOON CATHETER SYSTEM
Cardiovascular
80d
Cleared
Oct 12, 2004
MODIFICATION TO POLARCATH PERIPHERAL DILATATION SYSTEM
Cardiovascular
22d
Cleared
Feb 10, 2004
POLARCATH PERIPHERAL DILATATION SYSTEM
Cardiovascular
84d
Cleared
Aug 29, 2003
POLARCATH PERIPHERAL BALLOON CATHETER SYSTEM
Cardiovascular
172d
Cleared
Feb 19, 2003
CVSI PERIPHERAL BALLOON CATHETER
Cardiovascular
127d
Cleared
Sep 20, 2002
CVSI PERIPHERAL BALLOON CATHETER
Cardiovascular
87d