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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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