Cardiac Recorders, Ltd. is one of 195 FDA 510(k) medical device manufacturers from United Kingdom in the dataset, ranked by real submission volume.
Cardiac Recorders, Ltd. - FDA 510(k) Cleared Devices
8
Total
8
Cleared
0
Denied
Cardiac Recorders, Ltd. has 8 FDA 510(k) cleared medical devices. Based in London, GB.
Historical record: 8 cleared submissions from 1985 to 1987. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Cardiac Recorders, Ltd. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Cardiac Recorders, Ltd.
8 devices
Cleared
Mar 20, 1987
CARDIAN III CR6A
Cardiovascular
108d
Cleared
Sep 12, 1986
CARDIAN II CR45A
Cardiovascular
136d
Cleared
Dec 11, 1985
CARDIORATER CR 51
Cardiovascular
98d
Cleared
Nov 19, 1985
CARDIORATER CR7
Cardiovascular
133d
Cleared
Nov 14, 1985
CR5 CARDIAC MONITOR
Cardiovascular
128d
Cleared
Nov 05, 1985
CR 280/45, CR281/4 DEFIBRILLATOR
Cardiovascular
119d
Cleared
Sep 16, 1985
2006, 2010, 2011, 2012(CARDIAC DC DEFIBRILLATOR)
Cardiovascular
77d
Cleared
Sep 16, 1985
CR26, CR26A, CR26B, CR26C(CARDIAC DC DEFIBRILLATO)
Cardiovascular
76d