Lidco, Ltd. is one of 164 FDA 510(k) medical device manufacturers from United Kingdom in the dataset, ranked by real submission volume.
Lidco, Ltd. - FDA 510(k) Cleared Devices
7
Total
7
Cleared
0
Denied
Lidco, Ltd. has 7 FDA 510(k) cleared medical devices. Based in London, GB.
Historical record: 7 cleared submissions from 1999 to 2017. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Lidco, Ltd. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Lidco, Ltd.
7 devices
Cleared
Jun 05, 2017
LiDCOunity v2 Hemodynamic Monitor
Cardiovascular
189d
Cleared
Mar 17, 2016
LiDCOunity Monitor
Cardiovascular
164d
Cleared
Aug 28, 2013
LIDCO CNAP MODULE
Cardiovascular
135d
Cleared
Mar 20, 2013
LIDCORAPID V2 MONITOR
Cardiovascular
236d
Cleared
Jan 09, 2003
LIDCOPLUS HEMODYNAMIC MONITOR SYSTEM, MODEL HM 70
Cardiovascular
41d
Cleared
Jun 14, 2001
PULSECO HEMODYNAMIC MONITOR CM71
Cardiovascular
160d
Cleared
Jan 08, 1999
LIDCO SYSTEM
Cardiovascular
925d