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LOGIQ 5 Basic User Manual i-3 Direction 2300002-100 Rev. 2 Revision History Table i-1: Reason for Change REVDATEREASON FOR CHANGE Rev. 1 March 19, 2002 Update to Initial Release Rev. 2 March 26, 2003 R 2.x.x Update Table i-2: List of Effective Pages PAGE NUMBER REVISION NUMBER PA G E N U M B E R REVISION NUMBER Title Page Rev.

2 9-1 thru 9-104 Rev. 2 Revision History i-3 and i-4 Rev. 2 10-1 thru 10-90 Rev. 2 Regulatory Requirements i-5 and i-6 Rev.

2 11-1 thru 11-46 Rev. 2 Table of Contents i-7 thru i-16 Rev. 2 12-1 thru 12-2 Rev. 2 1-1 thru 1-12 Rev. 2 13-1 thru 13-10 Rev. 2 2-1 thru 2-32 Rev.

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2 18-1 thru 18-44 Rev. 2 7-1 thru 7-94 Rev. 2 Index 1 thru 8 Rev. 2 8-1 thru 8-22 Rev. 2 Please verify that you are using the latest revision of this document. Information pertaining to this document is maintained on GPC (GE Medical Systems Global Product Configuration). If you need to know the latest revision, contact your distributor, local GE Sales Representative or in the USA call the GE Ultrasound Clinical Answer Center at 1 800 682 5327 or 1 262 524 5698.