FDA 510(k) Applications Submitted by D. DUERSTELER

FDA 510(k) Number Submission Date Device Name Applicant
K960700 02/20/1996 LOGIQ A200 DIAGNOSTIC ULTRASOUND SYSTEM GE MEDICAL SYSTEMS
K062393 08/16/2006 GE VANTAGE PET NEURO SOFTWARE GE HEALTHCARE
K042866 10/18/2004 AMX5 AND AMX5D MOBILE X-RAY SYSTEMS GE HEALTHCARE TECHNOLOGIES
K014058 12/10/2001 ENTEGRA PE PERSONAL DIGITAL ASSISTANT GENERAL ELECTRIC MEDICAL SYSTEMS


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