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FDA 510(k) Applications Submitted by ROBERT F LAWRENCE
FDA 510(k) Number
Submission Date
Device Name
Applicant
K072365
08/23/2007
SEQUOIA PLUS DIAGNOSTIC ULTRASOUND SYSTEM
SIEMENS MEDICAL SOLUTIONS USA, INC., ULTRASOUND DI
K052355
08/29/2005
AUTOMATED BREAST ULTRASOUND SYSTEM, MODEL ABUS
U-SYSTEMS, INC.
K113179
10/28/2011
ACUSON SC2000 DIAGNOSTIC ULTRASOUND SYSTEM
SIEMENS MEDICAL SOLUTIONS USA, INC., ULTRASOUND DI
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