Bacchus Vascular, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Bacchus Vascular, Inc. - FDA 510(k) Cleared Devices
10
Total
10
Cleared
0
Denied
Bacchus Vascular, Inc. has 10 FDA 510(k) cleared cardiovascular devices. Based in Santa Clara, US.
Historical record: 10 cleared submissions from 2001 to 2008.
Browse the complete list of FDA 510(k) cleared cardiovascular devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Bacchus Vascular, Inc.
10 devices
Cleared
Oct 17, 2008
SPIRALFUSE PERIPHERAL INFUSION SYSTEM
Cardiovascular
74d
Cleared
Jul 13, 2007
TRELLIS-6 PERIPHERAL INFUSION SYSTEM
Cardiovascular
25d
Cleared
Feb 03, 2005
TRELLIS-8 PERIPHERAL INFUSION SYSTEM
Cardiovascular
10d
Cleared
Feb 04, 2004
SOLERA PLUS THROMBECTOMY CATHETER, 55 CM AND 110 CM, MODELS BAC SMG 007 055,...
Cardiovascular
42d
Cleared
Aug 22, 2003
Trellis Reserve Infusion System
Cardiovascular
30d
Cleared
Dec 02, 2002
SOLERA MAGNUM THROMBECTOMY CATHETER, 55 CM, MODEL BAC SMG 007 055 & SOLERA...
Cardiovascular
116d
Cleared
Dec 02, 2002
TRELLIS-6 PERIPHERAL INFUSION SYSTEM (140CM CATHETER LENGTH 10CM INFUSION...
Cardiovascular
42d
Cleared
Jul 03, 2002
TRELLIS PLUS INFUSION SYSTEM (140CM CATHETER LENGTH 10CM INFUSION LENGTH 20CM...
Cardiovascular
19d
Cleared
Feb 11, 2002
TRELLIS INFUSION SYSTEM (10CM INFUSION LENGTH)
Cardiovascular
98d
Cleared
Jun 06, 2001
BACCHUS THROMBECTOMY CATHETER (BTC), MODEL BTC-0755
Cardiovascular
198d