FDA 510(k) Applications Submitted by ROBERT 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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