Cobe Cardiovascular, Inc. - FDA 510(k) Cleared Devices
43
Total
43
Cleared
0
Denied
Cobe Cardiovascular, Inc. has 43 FDA 510(k) cleared cardiovascular devices. Based in Arvada, US.
Historical record: 43 cleared submissions from 1992 to 2005.
Browse the complete list of FDA 510(k) cleared cardiovascular devices from this manufacturer. Filter by specialty or product code using the sidebar.
43 devices
Cleared
Mar 08, 2005
SMARXT BMR 1900 CLOSED VENOUS RESERVOIR BAG
Cardiovascular
49d
Cleared
Nov 19, 2004
COBE ANGEL WHOLE BLOOD SEPARATION SYSTEM
Hematology
67d
Cleared
Feb 26, 2004
DIDECO MICRO 40 PH.I.S.I.O. ADULT ARTERIAL FILTER
Cardiovascular
31d
Cleared
Dec 11, 2003
SMARXT VVR4000I PLUS FILTERED HARDSHELL VENOUS RESERVOIR, MODEL 439914800
Cardiovascular
21d
Cleared
Mar 06, 2003
COBE REVOLUTION CENTRIFUGAL BLOOD PUMP WITH PC, MODEL 050300700
Cardiovascular
22d
Cleared
Jul 02, 2002
SORIN BIOMEDICA SMARXT BCD VANGUARD SURFACE MODIFIED CARDIOPLEGIA SYSTEM
Cardiovascular
28d
Cleared
Feb 12, 2002
COBE REVOLUTION
Cardiovascular
245d
Cleared
Nov 16, 2001
COBE SMARXT OPTIMIN SURFACE MODIFIED HOLLOW FIBER MEMBRANE OXYGENATOR
Cardiovascular
28d
Cleared
Nov 15, 2001
SORIN BIOMEDICA SMART BCD VANGUARD,SURFACE MODIFIED BLOOD CARDIOPLEGIA SYSTEM
Cardiovascular
90d
Cleared
Oct 26, 2001
STOCKERT V172 SERIES VENOUS FEMORAL CANNULAE
Cardiovascular
529d
Cleared
Sep 17, 2001
MODIFICATION TO: CSC14 BLOOD CARDIOPLEGIA SYSTEM
Cardiovascular
19d
Cleared
Apr 26, 2001
COBE VVR 4000 FILTERED HARDSHELL VENOUS RESERVOIR, COBE SMARXT VVR 4000...
Cardiovascular
118d
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