Cardiovascular Devices, Inc. - FDA 510(k) Cleared Devices
8
Total
8
Cleared
0
Denied
Cardiovascular Devices, Inc. has 8 FDA 510(k) cleared medical devices. Based in Walker, US.
Historical record: 8 cleared submissions from 1982 to 1989. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Cardiovascular Devices, Inc. Filter by specialty or product code using the sidebar.
8 devices
Cleared
May 23, 1989
THE CDI(R) SYSTEM 400
Toxicology
132d
Cleared
Jan 30, 1989
CDI(R) 2000 BLOOD GAS MONITOR
Anesthesiology
115d
Cleared
Jun 05, 1987
CDI(TM) EXTRACORPOREAL BLOOD GAS SYSTEM 300
Cardiovascular
70d
Cleared
Feb 19, 1987
MODIFIED GAS-STAT(TM) MONITORING SYSTEM
Cardiovascular
79d
Cleared
Jan 10, 1985
INTRAVASCULAR BLOOD GAS SYSTEM
Anesthesiology
99d
Cleared
Apr 17, 1984
GAST STAT MONITORING SYSTEM
Cardiovascular
54d
Cleared
May 27, 1983
GAS-STAT MONITORING SYSTEM
Cardiovascular
42d
Cleared
Dec 22, 1982
EXTRACORPOREAL BLOOD GAS SYSTEM
Cardiovascular
168d