ClearanceBrief
Company ยท GB

Lidco, Ltd.

FDA 510(k) clearances and medical device recalls filed under this name, 1999 to 2017. Name variants (Inc, Corp, punctuation) are merged.

7510(k) clearances (0 in 12 months)
1recalls (0 in 12 months)
1recalls that name a 510(k)

Product codes

CodeDeviceRecords
DXGComputer, Diagnostic, Pre-Programmed, Single-Function8

Latest 510(k) clearances

Decided510(k)Device and applicantCode
Jun 5, 2017K163334LiDCOunity v2 Hemodynamic Monitor
Lidco, Ltd., GB
DXG
Mar 17, 2016K152935LiDCOunity Monitor
Lidco, Ltd., GB
DXG
Aug 28, 2013K131048LIDCO CNAP MODULE
Lidco, Ltd., GB
DXG
Mar 20, 2013K122247LIDCORAPID V2 MONITOR
Lidco, Ltd., GB
DXG
Jan 9, 2003K023960LIDCOPLUS HEMODYNAMIC MONITOR SYSTEM, MODEL HM 70
Lidco, Ltd., GB
DXG
Jun 14, 2001K010049PULSECO HEMODYNAMIC MONITOR CM71
Lidco, Ltd., GB
DXG
Jan 8, 1999K962918LIDCO SYSTEM
Lidco, Ltd.
DXG

Latest recalls

DateFirm and productCodeLinked 510(k)
Nov 19, 2020Lidco Ltd
CM 50-001-01 Injectate Kit, accessory device to LiDCOunity v2 Monitor - Product Usage: intended to administer lithium dilution indicator (tube administrative set).
Terminated
DXGK163334
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