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FDA 510(k) Applications Submitted by GE MEDICAL SYSTEMS INFORMATION TECHNOLOGIES GMBH
FDA 510(k) Number
Submission Date
Device Name
Applicant
K103678
12/16/2010
CASE CARDIAC TESTING SYSTEM, CS CARDIAC TESTING SYSTEM
GE MEDICAL SYSTEMS INFORMATION TECHNOLOGIES GMBH
K000638
02/25/2000
RESPONDER 3000
GE MEDICAL SYSTEMS INFORMATION TECHNOLOGIES GMBH
K091594
06/02/2009
HEART-EXERCISE
GE MEDICAL SYSTEMS INFORMATION TECHNOLOGIES GMBH
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